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rs876657638

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657638(C;T)
Make rs876657638(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position7571554
GeneDSP
is asnp
is mentioned by
dbSNPrs876657638
ebirs876657638
HLIrs876657638
Exacrs876657638
Varsomers876657638
Maprs876657638
PheGenIrs876657638
hapmaprs876657638
1000 genomesrs876657638
hgdprs876657638
ensemblrs876657638
gopubmedrs876657638
geneviewrs876657638
scholarrs876657638
googlers876657638
pharmgkbrs876657638
gwascentralrs876657638
openSNPrs876657638
23andMers876657638
23andMe allrs876657638
SNP Nexus

SNPshotrs876657638
SNPdbers876657638
MSV3drs876657638
GWAS Ctlgrs876657638
Max Magnitude0
ClinVar
Risk rs876657638(T;T)
Alt rs876657638(T;T)
Reference rs876657638(C;C)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000006.11:g.7571787C>T
CLNSRC
CLNACC RCV000214415.1,