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rs762814879

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762814879(A;A)
Make rs762814879(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2528019
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs762814879
ebirs762814879
HLIrs762814879
Exacrs762814879
Varsomers762814879
Maprs762814879
PheGenIrs762814879
hapmaprs762814879
1000 genomesrs762814879
hgdprs762814879
ensemblrs762814879
gopubmedrs762814879
geneviewrs762814879
scholarrs762814879
googlers762814879
pharmgkbrs762814879
gwascentralrs762814879
openSNPrs762814879
23andMers762814879
23andMe allrs762814879
SNP Nexus

SNPshotrs762814879
SNPdbers762814879
MSV3drs762814879
GWAS Ctlgrs762814879
Max Magnitude0
ClinVar
Risk rs762814879(A;A)
Alt rs762814879(A;A)
Reference rs762814879(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2549249G>A
CLNSRC
CLNACC RCV000182253.2,