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rs794728544

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728544(A;T)
Make rs794728544(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2445135
GeneKCNQ1, LOC105376521
is asnp
is mentioned by
dbSNPrs794728544
ebirs794728544
HLIrs794728544
Exacrs794728544
Varsomers794728544
Maprs794728544
PheGenIrs794728544
hapmaprs794728544
1000 genomesrs794728544
hgdprs794728544
ensemblrs794728544
gopubmedrs794728544
geneviewrs794728544
scholarrs794728544
googlers794728544
pharmgkbrs794728544
gwascentralrs794728544
openSNPrs794728544
23andMers794728544
23andMe allrs794728544
SNP Nexus

SNPshotrs794728544
SNPdbers794728544
MSV3drs794728544
GWAS Ctlgrs794728544
Max Magnitude0
ClinVar
Risk rs794728544(T;T)
Alt rs794728544(T;T)
Reference rs794728544(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2466365A>T
CLNSRC
CLNACC RCV000182243.2,