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rs121917820

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917820(C;T)
Make rs121917820(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31117017
GeneCDSN, PSORS1C1
is asnp
is mentioned by
dbSNPrs121917820
ebirs121917820
HLIrs121917820
Exacrs121917820
Varsomers121917820
Maprs121917820
PheGenIrs121917820
hapmaprs121917820
1000 genomesrs121917820
hgdprs121917820
ensemblrs121917820
gopubmedrs121917820
geneviewrs121917820
scholarrs121917820
googlers121917820
pharmgkbrs121917820
gwascentralrs121917820
openSNPrs121917820
23andMers121917820
23andMe allrs121917820
SNP Nexus

SNPshotrs121917820
SNPdbers121917820
MSV3drs121917820
GWAS Ctlgrs121917820
Max Magnitude0
ClinVar
Risk rs121917820(T;T)
Alt rs121917820(T;T)
Reference rs121917820(C;C)
Significance Pathogenic
Disease Hypotrichosis 2
Variation info
Gene CDSN PSORS1C1
CLNDBN Hypotrichosis 2
Reversed 1
HGVS NC_000006.11:g.31084794G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007413.3,