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rs2637496

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2637496(C;T)
Make rs2637496(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position125407574
is asnp
is mentioned by
dbSNPrs2637496
ebirs2637496
HLIrs2637496
Exacrs2637496
Varsomers2637496
Maprs2637496
PheGenIrs2637496
hapmaprs2637496
1000 genomesrs2637496
hgdprs2637496
ensemblrs2637496
gopubmedrs2637496
geneviewrs2637496
scholarrs2637496
googlers2637496
pharmgkbrs2637496
gwascentralrs2637496
openSNPrs2637496
23andMers2637496
23andMe allrs2637496
SNP Nexus

SNPshotrs2637496
SNPdbers2637496
MSV3drs2637496
GWAS Ctlgrs2637496
GMAF0.1552
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20041166OA-icon.png]
Trait HIV-1 control
Title Common Genetic Variation and the Control of HIV-1 in Human
Risk Allele
P-val 0.000009
Odds Ratio NR NR