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rs766616232

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766616232(C;T)
Make rs766616232(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2587642
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs766616232
ebirs766616232
HLIrs766616232
Exacrs766616232
Varsomers766616232
Maprs766616232
PheGenIrs766616232
hapmaprs766616232
1000 genomesrs766616232
hgdprs766616232
ensemblrs766616232
gopubmedrs766616232
geneviewrs766616232
scholarrs766616232
googlers766616232
pharmgkbrs766616232
gwascentralrs766616232
openSNPrs766616232
23andMers766616232
23andMe allrs766616232
SNP Nexus

SNPshotrs766616232
SNPdbers766616232
MSV3drs766616232
GWAS Ctlgrs766616232
Max Magnitude0
ClinVar
Risk rs766616232(T;T)
Alt rs766616232(T;T)
Reference rs766616232(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2608872C>T
CLNSRC
CLNACC RCV000182317.1,