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rs794728562

From SNPedia

Orientationplus
Make rs794728562(-;-)
Make rs794728562(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2776986
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728562
ebirs794728562
HLIrs794728562
Exacrs794728562
Varsomers794728562
Maprs794728562
PheGenIrs794728562
hapmaprs794728562
1000 genomesrs794728562
hgdprs794728562
ensemblrs794728562
gopubmedrs794728562
geneviewrs794728562
scholarrs794728562
googlers794728562
pharmgkbrs794728562
gwascentralrs794728562
openSNPrs794728562
23andMers794728562
23andMe allrs794728562
SNP Nexus

SNPshotrs794728562
SNPdbers794728562
MSV3drs794728562
GWAS Ctlgrs794728562
Max Magnitude
ClinVar
Risk rs794728562(;)
Alt rs794728562(;)
Reference rs794728562(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2798216delG
CLNSRC
CLNACC RCV000182285.2,