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rs794728572

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728572(A;A)
Make rs794728572(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2587617
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728572
ebirs794728572
HLIrs794728572
Exacrs794728572
Varsomers794728572
Maprs794728572
PheGenIrs794728572
hapmaprs794728572
1000 genomesrs794728572
hgdprs794728572
ensemblrs794728572
gopubmedrs794728572
geneviewrs794728572
scholarrs794728572
googlers794728572
pharmgkbrs794728572
gwascentralrs794728572
openSNPrs794728572
23andMers794728572
23andMe allrs794728572
SNP Nexus

SNPshotrs794728572
SNPdbers794728572
MSV3drs794728572
GWAS Ctlgrs794728572
Max Magnitude0
ClinVar
Risk rs794728572(A;A)
Alt rs794728572(A;A)
Reference rs794728572(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2608847G>A
CLNSRC
CLNACC RCV000182315.1,