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rs7677751

From SNPedia

Orientationplus
Stabilizedplus
Make rs7677751(C;C)
Make rs7677751(C;T)
Make rs7677751(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position54258293
GenePDGFRA
is asnp
is mentioned by
dbSNPrs7677751
ebirs7677751
HLIrs7677751
Exacrs7677751
Varsomers7677751
Maprs7677751
PheGenIrs7677751
hapmaprs7677751
1000 genomesrs7677751
hgdprs7677751
ensemblrs7677751
gopubmedrs7677751
geneviewrs7677751
scholarrs7677751
googlers7677751
pharmgkbrs7677751
gwascentralrs7677751
openSNPrs7677751
23andMers7677751
23andMe allrs7677751
SNP Nexus

SNPshotrs7677751
SNPdbers7677751
MSV3drs7677751
GWAS Ctlgrs7677751
GMAF0.2163
Max Magnitude
? (C;C) (C;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 T
P-val 8E-9
Odds Ratio 1.2600 None

[PMID 18978678OA-icon.png] Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.