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rs1057519015

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519015(-;-)
Make rs1057519015(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position73325404
GeneHCN4
is asnp
is mentioned by
dbSNPrs1057519015
dbSNP (old)rs1057519015
ClinGenrs1057519015
ebirs1057519015
HLIrs1057519015
Exacrs1057519015
Gnomadrs1057519015
Varsomers1057519015
Maprs1057519015
PheGenIrs1057519015
Biobankrs1057519015
1000 genomesrs1057519015
hgdprs1057519015
ensemblrs1057519015
gopubmedrs1057519015
geneviewrs1057519015
scholarrs1057519015
googlers1057519015
pharmgkbrs1057519015
gwascentralrs1057519015
openSNPrs1057519015
23andMers1057519015
23andMe allrs1057519015
SNPshotrs1057519015
SNPdbers1057519015
MSV3drs1057519015
GWAS Ctlgrs1057519015
Max Magnitude0
ClinVar
Risk rs1057519015(-;-)
Alt rs1057519015(-;-)
Reference Rs1057519015(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.73617745delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000005482.2,