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rs979976

From SNPedia

Orientationplus
Stabilizedplus
Make rs979976(A;A)
Make rs979976(A;C)
Make rs979976(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position137011132
GeneTHSD7B
is asnp
is mentioned by
dbSNPrs979976
ebirs979976
HLIrs979976
Exacrs979976
Varsomers979976
Maprs979976
PheGenIrs979976
hapmaprs979976
1000 genomesrs979976
hgdprs979976
ensemblrs979976
gopubmedrs979976
geneviewrs979976
scholarrs979976
googlers979976
pharmgkbrs979976
gwascentralrs979976
openSNPrs979976
23andMers979976
23andMe allrs979976
SNP Nexus

SNPshotrs979976
SNPdbers979976
MSV3drs979976
GWAS Ctlgrs979976
GMAF0.3944
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 8E-6
Odds Ratio .13 [0.075-0.193] unit increase