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rs1057519276

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519276(C;G)
Make rs1057519276(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position73332261
GeneHCN4
is asnp
is mentioned by
dbSNPrs1057519276
dbSNP (old)rs1057519276
ClinGenrs1057519276
ebirs1057519276
HLIrs1057519276
Exacrs1057519276
Gnomadrs1057519276
Varsomers1057519276
Maprs1057519276
PheGenIrs1057519276
Biobankrs1057519276
1000 genomesrs1057519276
hgdprs1057519276
ensemblrs1057519276
gopubmedrs1057519276
geneviewrs1057519276
scholarrs1057519276
googlers1057519276
pharmgkbrs1057519276
gwascentralrs1057519276
openSNPrs1057519276
23andMers1057519276
23andMe allrs1057519276
SNPshotrs1057519276
SNPdbers1057519276
MSV3drs1057519276
GWAS Ctlgrs1057519276
Max Magnitude0
ClinVar
Risk rs1057519276(G;G)
Alt rs1057519276(G;G)
Reference Rs1057519276(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.73624602G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000415571.1,