Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894485

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894485(A;A)
Make rs104894485(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position73325378
GeneHCN4
is asnp
is mentioned by
dbSNPrs104894485
ebirs104894485
HLIrs104894485
Exacrs104894485
Varsomers104894485
Maprs104894485
PheGenIrs104894485
hapmaprs104894485
1000 genomesrs104894485
hgdprs104894485
ensemblrs104894485
gopubmedrs104894485
geneviewrs104894485
scholarrs104894485
googlers104894485
pharmgkbrs104894485
gwascentralrs104894485
openSNPrs104894485
23andMers104894485
23andMe allrs104894485
SNP Nexus

SNPshotrs104894485
SNPdbers104894485
MSV3drs104894485
GWAS Ctlgrs104894485
Max Magnitude0
OMIM605206
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894485(A;A)
Alt rs104894485(A;A)
Reference rs104894485(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.73617719C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005483.2,