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rs794728378

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728378(A;G)
Make rs794728378(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951480
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728378
ebirs794728378
HLIrs794728378
Exacrs794728378
Varsomers794728378
Maprs794728378
PheGenIrs794728378
hapmaprs794728378
1000 genomesrs794728378
hgdprs794728378
ensemblrs794728378
gopubmedrs794728378
geneviewrs794728378
scholarrs794728378
googlers794728378
pharmgkbrs794728378
gwascentralrs794728378
openSNPrs794728378
23andMers794728378
23andMe allrs794728378
SNP Nexus

SNPshotrs794728378
SNPdbers794728378
MSV3drs794728378
GWAS Ctlgrs794728378
Max Magnitude0
ClinVar
Risk rs794728378(G;G)
Alt rs794728378(G;G)
Reference rs794728378(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648568T>C
CLNSRC
CLNACC RCV000181828.1,