List of variants reported as uncertain significance for susceptibility to HIV infection by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_021155.4(CD209):c.642G>C (p.Glu214Asp)	rs11465377	0.01020
NM_001171174.1(CX3CR1):c.10C>G (p.Pro4Ala)	rs147724093	0.00570
NM_000634.3(CXCR1):c.3G>A (p.Met1Ile)	rs55808468	0.00533
NM_000418.4(IL4R):c.1160C>T (p.Ser387Leu)	rs6413500	0.00374
NM_000572.3(IL10):c.43G>A (p.Gly15Arg)	rs145922845	0.00186
NM_000418.4(IL4R):c.1774G>T (p.Val592Leu)	rs138392496	0.00156
NM_001394783.1(CCR5):c.187A>T (p.Ser63Cys)	rs142829420	0.00065
NM_003265.3(TLR3):c.554C>T (p.Ala185Val)	rs35140061	0.00048
NM_000634.3(CXCR1):c.608G>A (p.Arg203Gln)	rs538588993	0.00017
NM_001123396.4(CCR2):c.1043C>T (p.Thr348Met)	rs779248623	0.00012
NM_199168.4(CXCL12):c.*2C>T	rs749856360	0.00003
NM_001123396.4(CCR2):c.*1179G>A	rs368150580	0.00001
NM_000634.3(CXCR1):c.838C>T (p.Arg280Cys)
NM_021155.4(CD209):c.566A>T (p.Gln189Leu)	rs749759932

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.