CHROMOSOME 6 INTERGENIC GENE VIEW INTERGENIC ?q23 ?q25 rs7746082 — ~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 rs7746082 G / A · INTERGENIC 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

rs7746082

Gene: INTERGENIC — Intergenic / Genome-wide Chr 6:105987394
NCBI ↗ GeneCards ↗ Open Targets ↗ gnomAD ↗ OMIM ↗ Varsome ↗ LOVD ↗

Population Frequencies11

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Total G 0.76668C 0.23332GG 0.599494GC/CG 0.334366CC 0.06614pop=84,608
African G 0.9669C 0.0331GG 0.937152GC/CG 0.059574CC 0.003273pop=6,110
African American G 0.9655C 0.0345GG 0.934359GC/CG 0.062222CC 0.003419pop=5,850
Asian G 0.9988C 0.0012GG 0.997558GC/CG 0.002442CC 0pop=3,276
East Asian G 0.9996C 0.0004GG 0.999245GC/CG 0.000755CC 0pop=2,650
European G 0.73419C 0.26581GG 0.544155GC/CG 0.380075CC 0.07577pop=71,928
Latin American 1 G 0.822C 0.178GG 0.695652GC/CG 0.252174CC 0.052174pop=460
Latin American 2 G 0.898C 0.102GG 0.819355GC/CG 0.156989CC 0.023656pop=930
Other G 0.8711C 0.1289GG 0.78777GC/CG 0.166667CC 0.045564pop=1,668
Other Asian G 0.995C 0.005GG 0.990415GC/CG 0.009585CC 0pop=626
South Asian G 0.898C 0.102GG 0.813559GC/CG 0.169492CC 0.016949pop=236

Studies2

Unread Studies2
1
PID
Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.
2
PID
Genetic susceptibility to inflammation and colonic transit in lower functional gastrointestinal disorders: preliminary analysis.
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.