ClinVar Miner

List of variants reported as protective for susceptibility to HIV infection

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000579.4(CCR5):c.-301+246A>G rs1799987 0.48765
NC_000017.11:g.34253212= rs1024610 0.15212
NM_002982.4(CCL2):c.77-109= rs2857657 0.14061
NC_000017.11:g.34284427= rs4795895 0.13788
NM_001123396.4(CCR2):c.190G>A (p.Val64Ile) rs1799864 0.11966
NM_001394783.1(CCR5):c.180G>T (p.Arg60Ser) rs1800940 0.00113
NM_001394783.1(CCR5):c.303T>A (p.Cys101Ter) rs1800560 0.00087
NM_001394783.1(CCR5):c.554_585del (p.Ser185fs) rs333
NM_003265.3(TLR3):c.1234C>T (p.Leu412Phe) rs3775291
NM_199168.4(CXCL12):c.*531G>A rs387906400

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.