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rs13189798

From SNPedia

Orientationplus
Stabilizedplus
Make rs13189798(A;A)
Make rs13189798(A;C)
Make rs13189798(C;C)
ReferenceGRCh38 38.1/142
Chromosome5
Position76191426
GeneSV2C
is asnp
is mentioned by
dbSNPrs13189798
ebirs13189798
HLIrs13189798
Exacrs13189798
Varsomers13189798
Maprs13189798
PheGenIrs13189798
hapmaprs13189798
1000 genomesrs13189798
hgdprs13189798
ensemblrs13189798
gopubmedrs13189798
geneviewrs13189798
scholarrs13189798
googlers13189798
pharmgkbrs13189798
gwascentralrs13189798
openSNPrs13189798
23andMers13189798
23andMe allrs13189798
SNP Nexus

SNPshotrs13189798
SNPdbers13189798
MSV3drs13189798
GWAS Ctlgrs13189798
Max Magnitude

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