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rs12960119

From SNPedia

Orientationplus
Stabilizedplus
Make rs12960119(A;A)
Make rs12960119(A;G)
Make rs12960119(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position26034739
GeneSS18
is asnp
is mentioned by
dbSNPrs12960119
ebirs12960119
HLIrs12960119
Exacrs12960119
Varsomers12960119
Maprs12960119
PheGenIrs12960119
hapmaprs12960119
1000 genomesrs12960119
hgdprs12960119
ensemblrs12960119
gopubmedrs12960119
geneviewrs12960119
scholarrs12960119
googlers12960119
pharmgkbrs12960119
gwascentralrs12960119
openSNPrs12960119
23andMers12960119
23andMe allrs12960119
SNP Nexus

SNPshotrs12960119
SNPdbers12960119
MSV3drs12960119
GWAS Ctlgrs12960119
GMAF0.2938
Max Magnitude
? (A;A) (A;G) (G;G) 28

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