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rs10189905

From SNPedia

Orientationplus
Stabilizedplus
Make rs10189905(G;G)
Make rs10189905(G;T)
Make rs10189905(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position198814386
is asnp
is mentioned by
dbSNPrs10189905
dbSNP (classic)rs10189905
ClinGenrs10189905
ebirs10189905
HLIrs10189905
Exacrs10189905
Gnomadrs10189905
Varsomers10189905
LitVarrs10189905
Maprs10189905
PheGenIrs10189905
Biobankrs10189905
1000 genomesrs10189905
hgdprs10189905
ensemblrs10189905
geneviewrs10189905
scholarrs10189905
googlers10189905
pharmgkbrs10189905
gwascentralrs10189905
openSNPrs10189905
23andMers10189905
SNPshotrs10189905
SNPdbers10189905
MSV3drs10189905
GWAS Ctlgrs10189905
GMAF0.1235
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GWAS snp
PMID [PMID 22144915OA-icon.png]
Trait
Title Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism.
Risk Allele
P-val 6E-7
Odds Ratio 1.3200 None