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rs794727637

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727637(A;A)
Make rs794727637(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position73329719
GeneHCN4
is asnp
is mentioned by
dbSNPrs794727637
ebirs794727637
HLIrs794727637
Exacrs794727637
Varsomers794727637
Maprs794727637
PheGenIrs794727637
hapmaprs794727637
1000 genomesrs794727637
hgdprs794727637
ensemblrs794727637
gopubmedrs794727637
geneviewrs794727637
scholarrs794727637
googlers794727637
pharmgkbrs794727637
gwascentralrs794727637
openSNPrs794727637
23andMers794727637
23andMe allrs794727637
SNP Nexus

SNPshotrs794727637
SNPdbers794727637
MSV3drs794727637
GWAS Ctlgrs794727637
Max Magnitude0
ClinVar
Risk rs794727637(A;A)
Alt rs794727637(A;A)
Reference rs794727637(G;G)
Significance Probable-Pathogenic
Disease Sick sinus syndrome 2
Variation info
Gene HCN4
CLNDBN Sick sinus syndrome 2, autosomal dominant
Reversed 1
HGVS NC_000015.9:g.73622060C>T
CLNSRC
CLNACC RCV000178241.1,