Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852782

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852782(G;G)
Make rs137852782(G;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31001724
GeneDSC3
is asnp
is mentioned by
dbSNPrs137852782
ebirs137852782
HLIrs137852782
Exacrs137852782
Varsomers137852782
Maprs137852782
PheGenIrs137852782
hapmaprs137852782
1000 genomesrs137852782
hgdprs137852782
ensemblrs137852782
gopubmedrs137852782
geneviewrs137852782
scholarrs137852782
googlers137852782
pharmgkbrs137852782
gwascentralrs137852782
openSNPrs137852782
23andMers137852782
23andMe allrs137852782
SNP Nexus

SNPshotrs137852782
SNPdbers137852782
MSV3drs137852782
GWAS Ctlgrs137852782
Max Magnitude0
OMIM600271
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137852782(G;G)
Alt rs137852782(G;G)
Reference rs137852782(T;T)
Significance Pathogenic
Disease Hypotrichosis and recurrent skin vesicles
Variation info
Gene DSC3
CLNDBN Hypotrichosis and recurrent skin vesicles
Reversed 1
HGVS NC_000018.9:g.28581690A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009812.3,