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rs200476515

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200476515(C;T)
Make rs200476515(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7566380
GeneDSP
is asnp
is mentioned by
dbSNPrs200476515
ebirs200476515
HLIrs200476515
Exacrs200476515
Varsomers200476515
Maprs200476515
PheGenIrs200476515
hapmaprs200476515
1000 genomesrs200476515
hgdprs200476515
ensemblrs200476515
gopubmedrs200476515
geneviewrs200476515
scholarrs200476515
googlers200476515
pharmgkbrs200476515
gwascentralrs200476515
openSNPrs200476515
23andMers200476515
23andMe allrs200476515
SNP Nexus

SNPshotrs200476515
SNPdbers200476515
MSV3drs200476515
GWAS Ctlgrs200476515
Max Magnitude0
ClinVar
Risk rs200476515(T;T)
Alt rs200476515(T;T)
Reference rs200476515(C;C)
Significance Probable-Pathogenic
Disease not specified Arrhythmogenic right ventricular cardiomyopathy Cardiomyopathy dilated with woolly hair and keratoderma
Variation info
Gene DSP
CLNDBN not specified Arrhythmogenic right ventricular cardiomyopathy, type 8 Cardiomyopathy dilated with woolly hair and keratoderma
Reversed 0
HGVS NC_000006.11:g.7566613C>T
CLNSRC
CLNACC RCV000038121.3, RCV000232142.1,