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rs267607477

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607477(A;A)
Make rs267607477(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position52567115
GeneKRT74
is asnp
is mentioned by
dbSNPrs267607477
ebirs267607477
HLIrs267607477
Exacrs267607477
Varsomers267607477
Maprs267607477
PheGenIrs267607477
hapmaprs267607477
1000 genomesrs267607477
hgdprs267607477
ensemblrs267607477
gopubmedrs267607477
geneviewrs267607477
scholarrs267607477
googlers267607477
pharmgkbrs267607477
gwascentralrs267607477
openSNPrs267607477
23andMers267607477
23andMe allrs267607477
SNP Nexus

SNPshotrs267607477
SNPdbers267607477
MSV3drs267607477
GWAS Ctlgrs267607477
Max Magnitude0
ClinVar
Risk rs267607477(A;A)
Alt rs267607477(A;A)
Reference rs267607477(G;G)
Significance Pathogenic
Disease Hypotrichosis 3 not provided
Variation info
Gene KRT74
CLNDBN Hypotrichosis 3 not provided
Reversed 1
HGVS NC_000012.11:g.52960899C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023697.6, RCV000057502.1,