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rs764781840

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs764781840(C;C)
Make rs764781840(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2572086
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs764781840
ebirs764781840
HLIrs764781840
Exacrs764781840
Varsomers764781840
Maprs764781840
PheGenIrs764781840
hapmaprs764781840
1000 genomesrs764781840
hgdprs764781840
ensemblrs764781840
gopubmedrs764781840
geneviewrs764781840
scholarrs764781840
googlers764781840
pharmgkbrs764781840
gwascentralrs764781840
openSNPrs764781840
23andMers764781840
23andMe allrs764781840
SNP Nexus

SNPshotrs764781840
SNPdbers764781840
MSV3drs764781840
GWAS Ctlgrs764781840
Max Magnitude0
ClinVar
Risk rs764781840(C,G;C,G)
Alt rs764781840(C,G;C,G)
Reference rs764781840(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2593316T>C
CLNSRC
CLNACC RCV000182107.1,