Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606777(C;T)
Make rs267606777(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31392200
GeneDSG4
is asnp
is mentioned by
dbSNPrs267606777
ebirs267606777
HLIrs267606777
Exacrs267606777
Varsomers267606777
Maprs267606777
PheGenIrs267606777
hapmaprs267606777
1000 genomesrs267606777
hgdprs267606777
ensemblrs267606777
gopubmedrs267606777
geneviewrs267606777
scholarrs267606777
googlers267606777
pharmgkbrs267606777
gwascentralrs267606777
openSNPrs267606777
23andMers267606777
23andMe allrs267606777
SNP Nexus

SNPshotrs267606777
SNPdbers267606777
MSV3drs267606777
GWAS Ctlgrs267606777
Max Magnitude0
ClinVar
Risk rs267606777(T;T)
Alt rs267606777(T;T)
Reference rs267606777(C;C)
Significance Pathogenic
Disease Hypotrichosis 6
Variation info
Gene DSG1-AS1 DSG4
CLNDBN Hypotrichosis 6
Reversed 0
HGVS NC_000018.9:g.28972163C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002845.2,