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rs794728408

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728408(A;A)
Make rs794728408(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974882
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728408
ebirs794728408
HLIrs794728408
Exacrs794728408
Varsomers794728408
Maprs794728408
PheGenIrs794728408
hapmaprs794728408
1000 genomesrs794728408
hgdprs794728408
ensemblrs794728408
gopubmedrs794728408
geneviewrs794728408
scholarrs794728408
googlers794728408
pharmgkbrs794728408
gwascentralrs794728408
openSNPrs794728408
23andMers794728408
23andMe allrs794728408
SNP Nexus

SNPshotrs794728408
SNPdbers794728408
MSV3drs794728408
GWAS Ctlgrs794728408
Max Magnitude0
ClinVar
Risk rs794728408(A;A)
Alt rs794728408(A;A)
Reference rs794728408(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150671970C>T
CLNSRC
CLNACC RCV000181928.2,