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rs794728476

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728476(-;ATCGCGCAG)
Make rs794728476(ATCGCGCAG;ATCGCGCAG)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974765
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728476
ClinGenrs794728476
ebirs794728476
HLIrs794728476
Exacrs794728476
Varsomers794728476
Maprs794728476
PheGenIrs794728476
hapmaprs794728476
1000 genomesrs794728476
hgdprs794728476
ensemblrs794728476
gopubmedrs794728476
geneviewrs794728476
scholarrs794728476
googlers794728476
pharmgkbrs794728476
gwascentralrs794728476
openSNPrs794728476
23andMers794728476
23andMe allrs794728476
SNP Nexus

SNPshotrs794728476
SNPdbers794728476
MSV3drs794728476
GWAS Ctlgrs794728476
Max Magnitude0
ClinVar
Risk rs794728476(ATCGCGCAG;ATCGCGCAG)
Alt rs794728476(ATCGCGCAG;ATCGCGCAG)
Reference Rs794728476(;)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150671854_150671862dupCTGCGCGAT
CLNSRC
CLNACC RCV000182016.1,