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rs267606775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606775(C;C)
Make rs267606775(C;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31390712
GeneDSG4
is asnp
is mentioned by
dbSNPrs267606775
ebirs267606775
HLIrs267606775
Exacrs267606775
Varsomers267606775
Maprs267606775
PheGenIrs267606775
hapmaprs267606775
1000 genomesrs267606775
hgdprs267606775
ensemblrs267606775
gopubmedrs267606775
geneviewrs267606775
scholarrs267606775
googlers267606775
pharmgkbrs267606775
gwascentralrs267606775
openSNPrs267606775
23andMers267606775
23andMe allrs267606775
SNP Nexus

SNPshotrs267606775
SNPdbers267606775
MSV3drs267606775
GWAS Ctlgrs267606775
Max Magnitude0
ClinVar
Risk rs267606775(A,C;A,C)
Alt rs267606775(A,C;A,C)
Reference rs267606775(T;T)
Significance Pathogenic
Disease Hypotrichosis 6
Variation info
Gene DSG1-AS1 DSG4
CLNDBN Hypotrichosis 6
Reversed 0
HGVS NC_000018.9:g.28970675T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002840.3,