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rs11889995

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs11889995(C;T)
Make rs11889995(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position51936272
GeneAC007682.1
is asnp
is mentioned by
dbSNPrs11889995
ebirs11889995
HLIrs11889995
Exacrs11889995
Varsomers11889995
Maprs11889995
PheGenIrs11889995
hapmaprs11889995
1000 genomesrs11889995
hgdprs11889995
ensemblrs11889995
gopubmedrs11889995
geneviewrs11889995
scholarrs11889995
googlers11889995
pharmgkbrs11889995
gwascentralrs11889995
openSNPrs11889995
23andMers11889995
23andMe allrs11889995
SNP Nexus

SNPshotrs11889995
SNPdbers11889995
MSV3drs11889995
GWAS Ctlgrs11889995
GMAF0.0225
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 22410552] Evaluation of SNPs on chromosome 2p with primary open angle glaucoma in the South Indian cohort [PMID 19805132OA-icon.png] Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados.