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rs794728486

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728486(A;A)
Make rs794728486(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951450
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728486
ebirs794728486
HLIrs794728486
Exacrs794728486
Varsomers794728486
Maprs794728486
PheGenIrs794728486
hapmaprs794728486
1000 genomesrs794728486
hgdprs794728486
ensemblrs794728486
gopubmedrs794728486
geneviewrs794728486
scholarrs794728486
googlers794728486
pharmgkbrs794728486
gwascentralrs794728486
openSNPrs794728486
23andMers794728486
23andMe allrs794728486
SNP Nexus

SNPshotrs794728486
SNPdbers794728486
MSV3drs794728486
GWAS Ctlgrs794728486
Max Magnitude0
ClinVar
Risk rs794728486(A;A)
Alt rs794728486(A;A)
Reference rs794728486(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648538C>T
CLNSRC
CLNACC RCV000182037.2,