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rs794728397

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728397(A;A)
Make rs794728397(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947801
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728397
ebirs794728397
HLIrs794728397
Exacrs794728397
Varsomers794728397
Maprs794728397
PheGenIrs794728397
hapmaprs794728397
1000 genomesrs794728397
hgdprs794728397
ensemblrs794728397
gopubmedrs794728397
geneviewrs794728397
scholarrs794728397
googlers794728397
pharmgkbrs794728397
gwascentralrs794728397
openSNPrs794728397
23andMers794728397
23andMe allrs794728397
SNP Nexus

SNPshotrs794728397
SNPdbers794728397
MSV3drs794728397
GWAS Ctlgrs794728397
Max Magnitude0
ClinVar
Risk rs794728397(A;A)
Alt rs794728397(A;A)
Reference rs794728397(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene KCNH2
CLNDBN not specified
Reversed 1
HGVS NC_000007.13:g.150644889C>T
CLNSRC
CLNACC RCV000181890.2,