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rs149089817

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149089817(A;A)
Make rs149089817(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2588797
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs149089817
ebirs149089817
HLIrs149089817
Exacrs149089817
Varsomers149089817
Maprs149089817
PheGenIrs149089817
hapmaprs149089817
1000 genomesrs149089817
hgdprs149089817
ensemblrs149089817
gopubmedrs149089817
geneviewrs149089817
scholarrs149089817
googlers149089817
pharmgkbrs149089817
gwascentralrs149089817
openSNPrs149089817
23andMers149089817
23andMe allrs149089817
SNP Nexus

SNPshotrs149089817
SNPdbers149089817
MSV3drs149089817
GWAS Ctlgrs149089817
Max Magnitude0
ClinVar
Risk rs149089817(A;A)
Alt rs149089817(A;A)
Reference rs149089817(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2610027G>A
CLNSRC
CLNACC RCV000182184.1,