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rs2071590

From SNPedia

Orientationminus
Stabilizedminus
Make rs2071590(C;C)
Make rs2071590(C;T)
Make rs2071590(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31571991
GeneLOC100287329, LTA
is asnp
is mentioned by
dbSNPrs2071590
ebirs2071590
HLIrs2071590
Exacrs2071590
Varsomers2071590
Maprs2071590
PheGenIrs2071590
hapmaprs2071590
1000 genomesrs2071590
hgdprs2071590
ensemblrs2071590
gopubmedrs2071590
geneviewrs2071590
scholarrs2071590
googlers2071590
pharmgkbrs2071590
gwascentralrs2071590
openSNPrs2071590
23andMers2071590
23andMe allrs2071590
SNP Nexus

SNPshotrs2071590
SNPdbers2071590
MSV3drs2071590
GWAS Ctlgrs2071590
GMAF0.3186
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24439028OA-icon.png] A search for age-related macular degeneration risk variants in Alzheimer disease genes and pathways


[PMID 16839190OA-icon.png] Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study.


[PMID 18704761OA-icon.png] Molecular genetics of myocardial infarction.


[PMID 18805939OA-icon.png] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.