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rs606231274

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs606231274(-;-)
Make rs606231274(-;GCCT)
Make rs606231274(GCCT;GCCT)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position31117447
GeneCDSN, PSORS1C1
is asnp
is mentioned by
dbSNPrs606231274
ebirs606231274
HLIrs606231274
Exacrs606231274
Varsomers606231274
Maprs606231274
PheGenIrs606231274
hapmaprs606231274
1000 genomesrs606231274
hgdprs606231274
ensemblrs606231274
gopubmedrs606231274
geneviewrs606231274
scholarrs606231274
googlers606231274
pharmgkbrs606231274
gwascentralrs606231274
openSNPrs606231274
23andMers606231274
23andMe allrs606231274
SNP Nexus

SNPshotrs606231274
SNPdbers606231274
MSV3drs606231274
GWAS Ctlgrs606231274
Max Magnitude0
ClinVar
Risk rs606231274(GCCT;GCCT)
Alt rs606231274(GCCT;GCCT)
Reference rs606231274(;)
Significance Pathogenic
Disease Peeling skin syndrome
Variation info
Gene CDSN PSORS1C1
CLNDBN Peeling skin syndrome
Reversed 1
HGVS NC_000006.11:g.31085225_31085228dupAGGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000144908.3,