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rs17312292

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common genotype
Make rs17312292(C;C)
Make rs17312292(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position175746470
is asnp
is mentioned by
dbSNPrs17312292
dbSNP (classic)rs17312292
ClinGenrs17312292
ebirs17312292
HLIrs17312292
Exacrs17312292
Gnomadrs17312292
Varsomers17312292
LitVarrs17312292
Maprs17312292
PheGenIrs17312292
Biobankrs17312292
1000 genomesrs17312292
hgdprs17312292
ensemblrs17312292
geneviewrs17312292
scholarrs17312292
googlers17312292
pharmgkbrs17312292
gwascentralrs17312292
openSNPrs17312292
23andMers17312292
SNPshotrs17312292
SNPdbers17312292
MSV3drs17312292
GWAS Ctlgrs17312292
GMAF0.01286
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 23322567OA-icon.png]
Trait Corneal astigmatism
Title Identification of a candidate gene for astigmatism.
Risk Allele C
P-val 7E-6
Odds Ratio .88 [NR] unit increase