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rs187531872

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs187531872(C;T)
Make rs187531872(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38608146
GeneSCN5A
is asnp
is mentioned by
dbSNPrs187531872
ebirs187531872
HLIrs187531872
Exacrs187531872
Varsomers187531872
Maprs187531872
PheGenIrs187531872
hapmaprs187531872
1000 genomesrs187531872
hgdprs187531872
ensemblrs187531872
gopubmedrs187531872
geneviewrs187531872
scholarrs187531872
googlers187531872
pharmgkbrs187531872
gwascentralrs187531872
openSNPrs187531872
23andMers187531872
23andMe allrs187531872
SNP Nexus

SNPshotrs187531872
SNPdbers187531872
MSV3drs187531872
GWAS Ctlgrs187531872
Max Magnitude0
ClinVar
Risk rs187531872(T;T)
Alt rs187531872(T;T)
Reference rs187531872(C;C)
Significance Pathogenic
Disease not specified Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene SCN5A
CLNDBN not specified Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000003.11:g.38649637C>T
CLNSRC
CLNACC RCV000151802.1, RCV000157496.1,