rs10226930

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common genotype

Make rs10226930(C;C)

Make rs10226930(C;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

156044601

is a	snp
is	mentioned by
dbSNP	rs10226930
dbSNP (classic)	rs10226930
ClinGen	rs10226930
ebi	rs10226930
HLI	rs10226930
Exac	rs10226930
Gnomad	rs10226930
Varsome	rs10226930
LitVar	rs10226930
Map	rs10226930
PheGenI	rs10226930
Biobank	rs10226930
1000 genomes	rs10226930
hgdp	rs10226930
ensembl	rs10226930
geneview	rs10226930
scholar	rs10226930
google	rs10226930
pharmgkb	rs10226930
gwascentral	rs10226930
openSNP	rs10226930
23andMe	rs10226930
SNPshot	rs10226930
SNPdbe	rs10226930
MSV3d	rs10226930
GWAS Ctlg	rs10226930

GMAF

0.06107

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 23322567]
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