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rs10226930

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Orientationplus
Stabilizedplus
Make rs10226930(C;C)
Make rs10226930(C;T)
Make rs10226930(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position156044601
is asnp
is mentioned by
dbSNPrs10226930
ebirs10226930
HLIrs10226930
Exacrs10226930
Varsomers10226930
Maprs10226930
PheGenIrs10226930
hapmaprs10226930
1000 genomesrs10226930
hgdprs10226930
ensemblrs10226930
gopubmedrs10226930
geneviewrs10226930
scholarrs10226930
googlers10226930
pharmgkbrs10226930
gwascentralrs10226930
openSNPrs10226930
23andMers10226930
23andMe allrs10226930
SNP Nexus

SNPshotrs10226930
SNPdbers10226930
MSV3drs10226930
GWAS Ctlgrs10226930
GMAF0.06107
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 C
P-val 8E-7
Odds Ratio 1.38 [NR] unit decrease