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rs387906841

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906841(A;T)
Make rs387906841(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31117440
GeneCDSN, PSORS1C1
is asnp
is mentioned by
dbSNPrs387906841
ebirs387906841
HLIrs387906841
Exacrs387906841
Varsomers387906841
Maprs387906841
PheGenIrs387906841
hapmaprs387906841
1000 genomesrs387906841
hgdprs387906841
ensemblrs387906841
gopubmedrs387906841
geneviewrs387906841
scholarrs387906841
googlers387906841
pharmgkbrs387906841
gwascentralrs387906841
openSNPrs387906841
23andMers387906841
23andMe allrs387906841
SNP Nexus

SNPshotrs387906841
SNPdbers387906841
MSV3drs387906841
GWAS Ctlgrs387906841
Max Magnitude0
ClinVar
Risk rs387906841(T;T)
Alt rs387906841(T;T)
Reference Rs387906841(A;A)
Significance Pathogenic
Disease Peeling skin syndrome
Variation info
Gene CDSN PSORS1C1
CLNDBN Peeling skin syndrome
Reversed 1
HGVS NC_000006.11:g.31085217T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023198.3,