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rs267606776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606776(C;G)
Make rs267606776(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31391193
GeneDSG4
is asnp
is mentioned by
dbSNPrs267606776
ebirs267606776
HLIrs267606776
Exacrs267606776
Varsomers267606776
Maprs267606776
PheGenIrs267606776
hapmaprs267606776
1000 genomesrs267606776
hgdprs267606776
ensemblrs267606776
gopubmedrs267606776
geneviewrs267606776
scholarrs267606776
googlers267606776
pharmgkbrs267606776
gwascentralrs267606776
openSNPrs267606776
23andMers267606776
23andMe allrs267606776
SNP Nexus

SNPshotrs267606776
SNPdbers267606776
MSV3drs267606776
GWAS Ctlgrs267606776
Max Magnitude0
ClinVar
Risk rs267606776(G;G)
Alt rs267606776(G;G)
Reference rs267606776(C;C)
Significance Pathogenic
Disease Hypotrichosis 6
Variation info
Gene DSG1-AS1 DSG4
CLNDBN Hypotrichosis 6
Reversed 0
HGVS NC_000018.9:g.28971156C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002843.2,