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rs104894488

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894488(A;A)
Make rs104894488(A;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position73324216
GeneHCN4
is asnp
is mentioned by
dbSNPrs104894488
ClinGenrs104894488
ebirs104894488
HLIrs104894488
Exacrs104894488
Varsomers104894488
Maprs104894488
PheGenIrs104894488
hapmaprs104894488
1000 genomesrs104894488
hgdprs104894488
ensemblrs104894488
gopubmedrs104894488
geneviewrs104894488
scholarrs104894488
googlers104894488
pharmgkbrs104894488
gwascentralrs104894488
openSNPrs104894488
23andMers104894488
23andMe allrs104894488
SNP Nexus

SNPshotrs104894488
SNPdbers104894488
MSV3drs104894488
GWAS Ctlgrs104894488
Max Magnitude0
OMIM605206
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894488(A;A) rs104894488(T;T)
Alt rs104894488(A;A) rs104894488(T;T)
Reference Rs104894488(C;C)
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.73616557G>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000005481.3,