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rs7651778

From SNPedia

Orientationplus
Stabilizedplus
Make rs7651778(C;C)
Make rs7651778(C;T)
Make rs7651778(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position156618766
is asnp
is mentioned by
dbSNPrs7651778
dbSNP (classic)rs7651778
ClinGenrs7651778
ebirs7651778
HLIrs7651778
Exacrs7651778
Gnomadrs7651778
Varsomers7651778
LitVarrs7651778
Maprs7651778
PheGenIrs7651778
Biobankrs7651778
1000 genomesrs7651778
hgdprs7651778
ensemblrs7651778
geneviewrs7651778
scholarrs7651778
googlers7651778
pharmgkbrs7651778
gwascentralrs7651778
openSNPrs7651778
23andMers7651778
SNPshotrs7651778
SNPdbers7651778
MSV3drs7651778
GWAS Ctlgrs7651778
GMAF0.4683
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23761726OA-icon.png]
Trait Corneal astigmatism
Title Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: Results of a genome-wide association study.
Risk Allele C
P-val 5E-6
Odds Ratio .13 [0.071-0.181] unit increase