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rs267606659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606659(G;G)
Make rs267606659(G;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position10455007
GeneAPCDD1
is asnp
is mentioned by
dbSNPrs267606659
ebirs267606659
HLIrs267606659
Exacrs267606659
Varsomers267606659
Maprs267606659
PheGenIrs267606659
hapmaprs267606659
1000 genomesrs267606659
hgdprs267606659
ensemblrs267606659
gopubmedrs267606659
geneviewrs267606659
scholarrs267606659
googlers267606659
pharmgkbrs267606659
gwascentralrs267606659
openSNPrs267606659
23andMers267606659
23andMe allrs267606659
SNP Nexus

SNPshotrs267606659
SNPdbers267606659
MSV3drs267606659
GWAS Ctlgrs267606659
Max Magnitude0
ClinVar
Risk rs267606659(G;G)
Alt rs267606659(G;G)
Reference rs267606659(T;T)
Significance Pathogenic
Disease Hypotrichosis simplex
Variation info
Gene APCDD1
CLNDBN Hypotrichosis simplex
Reversed 0
HGVS NC_000018.9:g.10455004T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003311.4,