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rs10502861

From SNPedia

Orientationplus
Stabilizedplus
Make rs10502861(C;C)
Make rs10502861(C;T)
Make rs10502861(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position45220183
GeneSLC14A2
is asnp
is mentioned by
dbSNPrs10502861
dbSNP (classic)rs10502861
ClinGenrs10502861
ebirs10502861
HLIrs10502861
Exacrs10502861
Gnomadrs10502861
Varsomers10502861
LitVarrs10502861
Maprs10502861
PheGenIrs10502861
Biobankrs10502861
1000 genomesrs10502861
hgdprs10502861
ensemblrs10502861
geneviewrs10502861
scholarrs10502861
googlers10502861
pharmgkbrs10502861
gwascentralrs10502861
openSNPrs10502861
23andMers10502861
SNPshotrs10502861
SNPdbers10502861
MSV3drs10502861
GWAS Ctlgrs10502861
GMAF0.3003
Max Magnitude0
? (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 C
P-val 3E-9
Odds Ratio 1.2800 None