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rs140474226

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140474226(C;T)
Make rs140474226(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7580370
GeneDSP
is asnp
is mentioned by
dbSNPrs140474226
ebirs140474226
HLIrs140474226
Exacrs140474226
Varsomers140474226
Maprs140474226
PheGenIrs140474226
hapmaprs140474226
1000 genomesrs140474226
hgdprs140474226
ensemblrs140474226
gopubmedrs140474226
geneviewrs140474226
scholarrs140474226
googlers140474226
pharmgkbrs140474226
gwascentralrs140474226
openSNPrs140474226
23andMers140474226
23andMe allrs140474226
SNP Nexus

SNPshotrs140474226
SNPdbers140474226
MSV3drs140474226
GWAS Ctlgrs140474226
Max Magnitude0
ClinVar
Risk rs140474226(T;T)
Alt rs140474226(T;T)
Reference rs140474226(C;C)
Significance Pathogenic
Disease not provided Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN not provided Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7580603C>T
CLNSRC
CLNACC RCV000149891.2, RCV000210378.1,