CHROMOSOME 7 DDC 7p12.2-p12.1 GENE VIEW DDC · 7p12.2-p12.1 7p13 7p11 rs6592961 — ~70,000 base pairs in the gene — ~14,000 uncommon variants · <1% of humans have them — ~1,000 common variants · >1% carry the alternate allele ALLELE STATE rs6592961 G / A · DDC · 7p12.2-p12.1 HOMOZYGOUS WILD TYPE (DOMINANT) 5′ 3′ G 5′ 3′ G HETEROZYGOUS 5′ 3′ G 5′ 3′ A HOMOZYGOUS ALTERNATE (RECESSIVE) 5′ 3′ A 5′ 3′ A G Guanine — reference allele A Adenine — variant allele genetics.jdge.cc

rs6592961

Gene: DDC — Dopa Decarboxylase Chr 7:50505192 7p12.2-p12.1 Intron Variant
NCBI ↗ Research Rabbit ↗ GeneCards ↗ Open Targets ↗ gnomAD ↗ OMIM ↗ Varsome ↗ LOVD ↗

Population Frequencies12

Sort by
Total G 0.769303A 0.230697GG 0.595378GA/AG 0.34785AA 0.056772pop=680,620
African G 0.63787A 0.36213GG 0.406242GA/AG 0.463262AA 0.130496pop=55,174
African American G 0.6389A 0.3611GG 0.407652GA/AG 0.46249AA 0.129858pop=53,212
African Others G 0.6101A 0.3899GG 0.367992GA/AG 0.4842AA 0.147808pop=1,962
Asian G 0.7944A 0.2056GG 0.63657GA/AG 0.31567AA 0.04776pop=11,474
East Asian G 0.782A 0.218GG 0.615116GA/AG 0.33377AA 0.051114pop=9,156
European G 0.787715A 0.212285GG 0.621281GA/AG 0.332867AA 0.045852pop=560,326
Latin American 1 G 0.7248A 0.2752GG 0.531302GA/AG 0.387023AA 0.081675pop=9,648
Latin American 2 G 0.61762A 0.38238GG 0.390367GA/AG 0.454515AA 0.155118pop=17,896
Other G 0.7562A 0.2438GG 0.57763GA/AG 0.357143AA 0.065227pop=18,060
Other Asian G 0.8434A 0.1566GG 0.721311GA/AG 0.244176AA 0.034513pop=2,318
South Asian G 0.7727A 0.2273GG 0.602338GA/AG 0.340711AA 0.056951pop=8,042

Studies20

Unread Studies20
1
Autism spectrum disorder (ASD) is a genetically heterogeneous syndrome characterized by repetitive, restricted, and stereotyped behaviors, along with persistent difficulties with social …
2
Работа Направлена На Описание Связи Генотипов Генов Катехол-О-Метилтрансферазы Comt, Дофаминового Рецептора Четвертого Типа Drd4, Серотонинового Рецептора …
3
… A recent study performed in a northern Spanish sample found a significant association between ASD and both the rs6592961 SNP and a four-marker haplotype in this gene [52]. …
4
Amaç: Dikkat eksikliği hiperaktivite bozukluğu (DEHB), çocuk psikiyatri hastalıkları arasında sıklıkla görülen bozukluklardandır. Atomoksetin DEHB tedavisinde tercih edilen ve bir …
5
It is inconclusive whether children with autism spectrum disorder (ASD) experience a deficit in facial emotion recognition. The dopaminergic pathway has been implicated …
6
El trastorno por déficit de atención e hiperactividad (TDAH) es uno de los desórdenes del neurodesarrollo infantil más frecuentes, afectando al 5, 3% de niños en edad escolar, cuyos …
7
La Leucemia linfoblástica aguda (LLA) infantil es el cáncer pediátrico más común. El hecho de que se desarrolle a una edad temprana sugiere que para su aparición debe existir un …
8
… and allele frequency of SNPs of DDC gene (rs6592961)and DRD1 (rs251937)gene in 97 … allele or genotype of SNPs of DDC gene(rs6592961)and DRD1 gene(rs251937)and the …
9
… rs6592961位点和DRD1基因rs251937位点等位基因频率和基因型分布上差异均无统计学 意义(P>0.05).②孤独症组病情轻中度与重度儿童DDC的rs6592961和… of DDC gene(rs6592961)and …
10
… We genotyped single-nucleotide polymorphisms rs6592961 and rs251937 in 211 autistic … Genotypes of DDC rs6592961 in the healthy control group were as follows: G/G 163 (65.2%)…
11
Populations exposed to Plasmodium falciparum infection develop genetic mechanisms of protection against severe malarial disease. Despite decades of genetic epidemiological …
12
Attention deficit hyperactivity disorder (ADHD) has a strong genetic component. The study is aimed to test the association of 34 polymorphisms with ADHD symptomatology …
13
… to determine genotype and allele of SNPs of DDC gene (rs6592961) and DRD1 (rs251937) gene in 97 … For DDC gene (rs6592961),significant difference was found in subscale between …
14
El trastorno por déficit de atención con hiperactividad (TDAH) es el trastorno neuropsiquiátrico más común en la infancia, con una prevalencia del 8 al 12% entre la población infanto-…
15
DOPA decarboxylase (DDC) is involved in the synthesis of dopamine, norepinephrine and serotonin. It has been suggested that genes involved in the dopamine, norepinephrine, and …
16
… The results of our case–control association study identified a single SNP (rs6592961) in the DOPA decarboxylase gene (DDC, 7p12.2) that remained significantly associated with …
17
Mauricio Arcos-Burgos and Maximilian Muenke n this chapter, we outline the role of evolutionary and epidemiological genetics for I dissecting and understanding attention through the …
18
Mauricio Arcos-Burgos and Maximilian Muenke n this chapter, we outline the role of evolutionary and epidemiological genetics for I dissecting and understanding attention through the …
19
… In summary, as shown in Figure 1, after correction for multiple testing, one SNP (rs6592961) within the DDC gene was associated with adult and child ADHD samples both when taking …
20
These are exciting times for genetics research: Science magazine chose our new appreciation of human genetic diversity as the scientific breakthrough of the year 2007.(1) The year …
Curated Studies0

These studies were determined to be useful for this variant — check "Unused Studies" further down if curious what didn't make the cut.

No curated studies yet.

Unused Studies0

No unused studies.