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rs121908411

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908411(C;C)
Make rs121908411(C;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position73329725
GeneHCN4
is asnp
is mentioned by
dbSNPrs121908411
ebirs121908411
HLIrs121908411
Exacrs121908411
Varsomers121908411
Maprs121908411
PheGenIrs121908411
hapmaprs121908411
1000 genomesrs121908411
hgdprs121908411
ensemblrs121908411
gopubmedrs121908411
geneviewrs121908411
scholarrs121908411
googlers121908411
pharmgkbrs121908411
gwascentralrs121908411
openSNPrs121908411
23andMers121908411
23andMe allrs121908411
SNP Nexus

SNPshotrs121908411
SNPdbers121908411
MSV3drs121908411
GWAS Ctlgrs121908411
Max Magnitude0
OMIM605206
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908411(C;C)
Alt rs121908411(C;C)
Reference rs121908411(G;G)
Significance Pathogenic
Disease Sick sinus syndrome 2
Variation info
Gene HCN4
CLNDBN Sick sinus syndrome 2, autosomal dominant
Reversed 1
HGVS NC_000015.9:g.73622066C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005484.2,