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rs876661350

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661350(A;A)
Make rs876661350(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position2570678
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs876661350
ebirs876661350
HLIrs876661350
Exacrs876661350
Varsomers876661350
Maprs876661350
PheGenIrs876661350
hapmaprs876661350
1000 genomesrs876661350
hgdprs876661350
ensemblrs876661350
gopubmedrs876661350
geneviewrs876661350
scholarrs876661350
googlers876661350
pharmgkbrs876661350
gwascentralrs876661350
openSNPrs876661350
23andMers876661350
23andMe allrs876661350
SNP Nexus

SNPshotrs876661350
SNPdbers876661350
MSV3drs876661350
GWAS Ctlgrs876661350
Max Magnitude0
ClinVar
Risk rs876661350(A;A)
Alt rs876661350(A;A)
Reference rs876661350(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2591908G>A
CLNSRC
CLNACC RCV000223822.1,