Have questions? Visit https://www.reddit.com/r/SNPedia

rs11223996

From SNPedia

Orientationplus
Stabilizedplus
Make rs11223996(C;C)
Make rs11223996(C;T)
Make rs11223996(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position134756993
GeneHSFX1
is asnp
is mentioned by
dbSNPrs11223996
ebirs11223996
HLIrs11223996
Exacrs11223996
Varsomers11223996
Maprs11223996
PheGenIrs11223996
hapmaprs11223996
1000 genomesrs11223996
hgdprs11223996
ensemblrs11223996
gopubmedrs11223996
geneviewrs11223996
scholarrs11223996
googlers11223996
pharmgkbrs11223996
gwascentralrs11223996
openSNPrs11223996
23andMers11223996
23andMe allrs11223996
SNP Nexus

SNPshotrs11223996
SNPdbers11223996
MSV3drs11223996
GWAS Ctlgrs11223996
GMAF0.1056
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23049088]
Trait Myopia (pathological)
Title A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
Risk Allele
P-val 7E-7
Odds Ratio NR NR