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rs606231294

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231294(C;T)
Make rs606231294(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7571471
GeneDSP
is asnp
is mentioned by
dbSNPrs606231294
ebirs606231294
HLIrs606231294
Exacrs606231294
Varsomers606231294
Maprs606231294
PheGenIrs606231294
hapmaprs606231294
1000 genomesrs606231294
hgdprs606231294
ensemblrs606231294
gopubmedrs606231294
geneviewrs606231294
scholarrs606231294
googlers606231294
pharmgkbrs606231294
gwascentralrs606231294
openSNPrs606231294
23andMers606231294
23andMe allrs606231294
SNP Nexus

SNPshotrs606231294
SNPdbers606231294
MSV3drs606231294
GWAS Ctlgrs606231294
Max Magnitude0
ClinVar
Risk rs606231294(T;T)
Alt rs606231294(T;T)
Reference rs606231294(C;C)
Significance Other
Disease Cardiomyopathy not provided
Variation info
Gene DSP
CLNDBN Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis not provided
Reversed 0
HGVS NC_000006.11:g.7571704C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144960.2, RCV000181378.1,