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rs606231295

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231295(C;T)
Make rs606231295(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7570553
GeneDSP
is asnp
is mentioned by
dbSNPrs606231295
ebirs606231295
HLIrs606231295
Exacrs606231295
Varsomers606231295
Maprs606231295
PheGenIrs606231295
hapmaprs606231295
1000 genomesrs606231295
hgdprs606231295
ensemblrs606231295
gopubmedrs606231295
geneviewrs606231295
scholarrs606231295
googlers606231295
pharmgkbrs606231295
gwascentralrs606231295
openSNPrs606231295
23andMers606231295
23andMe allrs606231295
SNP Nexus

SNPshotrs606231295
SNPdbers606231295
MSV3drs606231295
GWAS Ctlgrs606231295
Max Magnitude0
ClinVar
Risk rs606231295(T;T)
Alt rs606231295(T;T)
Reference Rs606231295(C;C)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene DSP
CLNDBN Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis
Reversed 0
HGVS NC_000006.11:g.7570786C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000144961.2,