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rs767643821

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767643821(C;T)
Make rs767643821(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7579995
GeneDSP
is asnp
is mentioned by
dbSNPrs767643821
ebirs767643821
HLIrs767643821
Exacrs767643821
Varsomers767643821
Maprs767643821
PheGenIrs767643821
hapmaprs767643821
1000 genomesrs767643821
hgdprs767643821
ensemblrs767643821
gopubmedrs767643821
geneviewrs767643821
scholarrs767643821
googlers767643821
pharmgkbrs767643821
gwascentralrs767643821
openSNPrs767643821
23andMers767643821
23andMe allrs767643821
SNP Nexus

SNPshotrs767643821
SNPdbers767643821
MSV3drs767643821
GWAS Ctlgrs767643821
Max Magnitude0
ClinVar
Risk rs767643821(A,T;A,T)
Alt rs767643821(A,T;A,T)
Reference rs767643821(C;C)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy Cardiomyopathy dilated with woolly hair and keratoderma not provided
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 8 Cardiomyopathy dilated with woolly hair and keratoderma not provided
Reversed 0
HGVS NC_000006.11:g.7580228C>A; NC_000006.11:g.7580228C>T
CLNSRC
CLNACC RCV000236353.1, RCV000181316.2,