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rs2497938

From SNPedia

Orientationplus
Stabilizedplus
Make rs2497938(C;C)
Make rs2497938(C;T)
Make rs2497938(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67343176
is asnp
is mentioned by
dbSNPrs2497938
ebirs2497938
HLIrs2497938
Exacrs2497938
Varsomers2497938
Maprs2497938
PheGenIrs2497938
hapmaprs2497938
1000 genomesrs2497938
hgdprs2497938
ensemblrs2497938
gopubmedrs2497938
geneviewrs2497938
scholarrs2497938
googlers2497938
pharmgkbrs2497938
gwascentralrs2497938
openSNPrs2497938
23andMers2497938
23andMe allrs2497938
SNP Nexus

SNPshotrs2497938
SNPdbers2497938
MSV3drs2497938
GWAS Ctlgrs2497938
GMAF0.3011
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22693459OA-icon.png]
Trait
Title Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
Risk Allele T
P-val 2E-91
Odds Ratio 2.2000 None


[PMID 22032556] Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness.