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rs794728574

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728574(A;T)
Make rs794728574(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2776000
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728574
ebirs794728574
HLIrs794728574
Exacrs794728574
Varsomers794728574
Maprs794728574
PheGenIrs794728574
hapmaprs794728574
1000 genomesrs794728574
hgdprs794728574
ensemblrs794728574
gopubmedrs794728574
geneviewrs794728574
scholarrs794728574
googlers794728574
pharmgkbrs794728574
gwascentralrs794728574
openSNPrs794728574
23andMers794728574
23andMe allrs794728574
SNP Nexus

SNPshotrs794728574
SNPdbers794728574
MSV3drs794728574
GWAS Ctlgrs794728574
Max Magnitude0
ClinVar
Risk rs794728574(T;T)
Alt rs794728574(T;T)
Reference rs794728574(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene KCNQ1
CLNDBN not specified
Reversed 0
HGVS NC_000011.9:g.2797230A>T
CLNSRC
CLNACC RCV000182321.2,