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rs113189798

From SNPedia

Orientationplus
Stabilizedplus
Make rs113189798(A;A)
Make rs113189798(A;G)
Make rs113189798(G;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position17385140
is asnp
is mentioned by
dbSNPrs113189798
dbSNP (old)rs113189798
ClinGenrs113189798
ebirs113189798
HLIrs113189798
Exacrs113189798
Gnomadrs113189798
Varsomers113189798
Maprs113189798
PheGenIrs113189798
Biobankrs113189798
1000 genomesrs113189798
hgdprs113189798
ensemblrs113189798
gopubmedrs113189798
geneviewrs113189798
scholarrs113189798
googlers113189798
pharmgkbrs113189798
gwascentralrs113189798
openSNPrs113189798
23andMers113189798
23andMe allrs113189798
SNP Nexus

SNPshotrs113189798
SNPdbers113189798
MSV3drs113189798
GWAS Ctlgrs113189798
Max Magnitude

[PMID 25985399OA-icon.png] Associations of common variants in the BST2 region with HIV-1 acquisition in African American and European American people who inject drugs