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rs6764388

From SNPedia

Orientationplus
Stabilizedplus
Make rs6764388(C;C)
Make rs6764388(C;T)
Make rs6764388(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position65341207
is asnp
is mentioned by
dbSNPrs6764388
ebirs6764388
HLIrs6764388
Exacrs6764388
Varsomers6764388
Maprs6764388
PheGenIrs6764388
hapmaprs6764388
1000 genomesrs6764388
hgdprs6764388
ensemblrs6764388
gopubmedrs6764388
geneviewrs6764388
scholarrs6764388
googlers6764388
pharmgkbrs6764388
gwascentralrs6764388
openSNPrs6764388
23andMers6764388
23andMe allrs6764388
SNP Nexus

SNPshotrs6764388
SNPdbers6764388
MSV3drs6764388
GWAS Ctlgrs6764388
GMAF0.3783
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23322567OA-icon.png]
Trait Corneal astigmatism
Title Identification of a candidate gene for astigmatism.
Risk Allele T
P-val 6E-6
Odds Ratio .05 [NR] unit increase