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

rs1057519275

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519275(C;C)
Make rs1057519275(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position73329722
GeneHCN4
is asnp
is mentioned by
dbSNPrs1057519275
dbSNP (old)rs1057519275
ClinGenrs1057519275
ebirs1057519275
HLIrs1057519275
Exacrs1057519275
Gnomadrs1057519275
Varsomers1057519275
Maprs1057519275
PheGenIrs1057519275
Biobankrs1057519275
1000 genomesrs1057519275
hgdprs1057519275
ensemblrs1057519275
gopubmedrs1057519275
geneviewrs1057519275
scholarrs1057519275
googlers1057519275
pharmgkbrs1057519275
gwascentralrs1057519275
openSNPrs1057519275
23andMers1057519275
23andMe allrs1057519275
SNPshotrs1057519275
SNPdbers1057519275
MSV3drs1057519275
GWAS Ctlgrs1057519275
Max Magnitude0
ClinVar
Risk rs1057519275(C;C)
Alt rs1057519275(C;C)
Reference Rs1057519275(T;T)
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.73622063A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000415538.1,