Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728527

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728527(A;A)
Make rs794728527(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2588844
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728527
ebirs794728527
HLIrs794728527
Exacrs794728527
Varsomers794728527
Maprs794728527
PheGenIrs794728527
hapmaprs794728527
1000 genomesrs794728527
hgdprs794728527
ensemblrs794728527
gopubmedrs794728527
geneviewrs794728527
scholarrs794728527
googlers794728527
pharmgkbrs794728527
gwascentralrs794728527
openSNPrs794728527
23andMers794728527
23andMe allrs794728527
SNP Nexus

SNPshotrs794728527
SNPdbers794728527
MSV3drs794728527
GWAS Ctlgrs794728527
Max Magnitude0
ClinVar
Risk rs794728527(A;A)
Alt rs794728527(A;A)
Reference rs794728527(T;T)
Significance Other
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2610074T>A
CLNSRC
CLNACC RCV000182178.1,