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rs775479779

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs775479779(A;A)
Make rs775479779(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2571362
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs775479779
ebirs775479779
HLIrs775479779
Exacrs775479779
Varsomers775479779
Maprs775479779
PheGenIrs775479779
hapmaprs775479779
1000 genomesrs775479779
hgdprs775479779
ensemblrs775479779
gopubmedrs775479779
geneviewrs775479779
scholarrs775479779
googlers775479779
pharmgkbrs775479779
gwascentralrs775479779
openSNPrs775479779
23andMers775479779
23andMe allrs775479779
SNP Nexus

SNPshotrs775479779
SNPdbers775479779
MSV3drs775479779
GWAS Ctlgrs775479779
Max Magnitude0
ClinVar
Risk rs775479779(A,T;A,T)
Alt rs775479779(A,T;A,T)
Reference rs775479779(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2592592C>A
CLNSRC
CLNACC RCV000182093.2,