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rs267738

From SNPedia

Orientationminus
Stabilizedminus
Make rs267738(A;A)
Make rs267738(A;C)
Make rs267738(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position150968149
GeneCERS2
is asnp
is mentioned by
dbSNPrs267738
ebirs267738
HLIrs267738
Exacrs267738
Varsomers267738
Maprs267738
PheGenIrs267738
hapmaprs267738
1000 genomesrs267738
hgdprs267738
ensemblrs267738
gopubmedrs267738
geneviewrs267738
scholarrs267738
googlers267738
pharmgkbrs267738
gwascentralrs267738
openSNPrs267738
23andMers267738
23andMe allrs267738
SNP Nexus

SNPshotrs267738
SNPdbers267738
MSV3drs267738
GWAS Ctlgrs267738
GMAF0.09917
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 23585552] Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment