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rs606231275

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231275(G;T)
Make rs606231275(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position31117191
GeneCDSN, PSORS1C1
is asnp
is mentioned by
dbSNPrs606231275
ebirs606231275
HLIrs606231275
Exacrs606231275
Varsomers606231275
Maprs606231275
PheGenIrs606231275
hapmaprs606231275
1000 genomesrs606231275
hgdprs606231275
ensemblrs606231275
gopubmedrs606231275
geneviewrs606231275
scholarrs606231275
googlers606231275
pharmgkbrs606231275
gwascentralrs606231275
openSNPrs606231275
23andMers606231275
23andMe allrs606231275
SNP Nexus

SNPshotrs606231275
SNPdbers606231275
MSV3drs606231275
GWAS Ctlgrs606231275
Max Magnitude0
ClinVar
Risk rs606231275(T;T)
Alt rs606231275(T;T)
Reference rs606231275(G;G)
Significance Pathogenic
Disease Peeling skin syndrome
Variation info
Gene CDSN PSORS1C1
CLNDBN Peeling skin syndrome
Reversed 1
HGVS NC_000006.11:g.31084968C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144909.3,