rs63750759
Arginine 1314 → Tryptophan
Gene: ABCC6 — ATP Binding Cassette Subfamily C Member 6
Chr 16:16154974
16p13.11
Missense Variant
Population Frequencies9
African
G 0.99839A 0.00161GG 0.996788GA/AG 0.003212AA 0pop=29,890
African American
G 0.99843A 0.00157GG 0.996853GA/AG 0.003147AA 0pop=28,596
African Others
G 0.9977A 0.0023GG 0.995363GA/AG 0.004637AA 0pop=1,294
Asian
G 0.9998A 0.0002GG 0.999666GA/AG 0.000334AA 0pop=5,986
East Asian
G 0.9998A 0.0002GG 0.999599GA/AG 0.000401AA 0pop=4,982
European
G 0.99998A 0.00002GG 0.99996GA/AG 0.00004AA 0pop=200,022
Latin American 2
G 0.9997A 0.0003GG 0.999404GA/AG 0.000596AA 0pop=3,354
Other
G 0.99972A 0.00028GG 0.999438GA/AG 0.000562AA 0pop=10,674
Studies1
Unread Studies1 ▼
1
Despite the existing data on the Multisystem Inflammatory Syndrome in Children (MIS-C), the factors that determine these patients evolution remain elusive. Answers may lie, at least in part, in genetics. It is currently under investigation that MIS-C patients may have an underlying innate error of immunity (IEI), whether of monogenic, digenic, or even oligogenic origin.
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.