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rs577948

From SNPedia

Orientationplus
Stabilizedplus
Make rs577948(A;A)
Make rs577948(A;G)
Make rs577948(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position122159482
GeneMIR100HG
is asnp
is mentioned by
dbSNPrs577948
ebirs577948
HLIrs577948
Exacrs577948
Varsomers577948
Maprs577948
PheGenIrs577948
hapmaprs577948
1000 genomesrs577948
hgdprs577948
ensemblrs577948
gopubmedrs577948
geneviewrs577948
scholarrs577948
googlers577948
pharmgkbrs577948
gwascentralrs577948
openSNPrs577948
23andMers577948
23andMe allrs577948
SNP Nexus

SNPshotrs577948
SNPdbers577948
MSV3drs577948
GWAS Ctlgrs577948
GMAF0.3632
Max Magnitude
Despite two previous GWAS studies associating this SNP with high myopia in Japanese populations, no association was seen in a Chinese population studied.[PMID 22194655OA-icon.png]
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19779542OA-icon.png]
Trait Myopia (pathological)
Title A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1
Risk Allele G
P-val 2E-7
Odds Ratio 1.37 [1.21-1.54]


GET Evidence
rs577948
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.382812
summary