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rs1136200

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1136200(A;A)
Make rs1136200(A;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position11810038
GeneLINC00687
is asnp
is mentioned by
dbSNPrs1136200
ebirs1136200
HLIrs1136200
Exacrs1136200
Varsomers1136200
Maprs1136200
PheGenIrs1136200
hapmaprs1136200
1000 genomesrs1136200
hgdprs1136200
ensemblrs1136200
gopubmedrs1136200
geneviewrs1136200
scholarrs1136200
googlers1136200
pharmgkbrs1136200
gwascentralrs1136200
openSNPrs1136200
23andMers1136200
23andMe allrs1136200
SNP Nexus

SNPshotrs1136200
SNPdbers1136200
MSV3drs1136200
GWAS Ctlgrs1136200
GMAF0.01653
Max Magnitude0
[PMID 18837888] and the risk of breast cancer