Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852488
rs137852488
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		C 0.810 CausalMutation CLINVAR

dbSNP: rs137852483
rs137852483
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		A 0.810 CausalMutation CLINVAR

dbSNP: rs387906725
rs387906725
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		A 0.800 CausalMutation CLINVAR

dbSNP: rs267606863
rs267606863
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137852504
rs137852504
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		G 0.800 CausalMutation CLINVAR

dbSNP: rs137852501
rs137852501
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		G 0.800 CausalMutation CLINVAR

dbSNP: rs137852500
rs137852500
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137852499
rs137852499
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137852498
rs137852498
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		T 0.800 CausalMutation CLINVAR

dbSNP: rs137852496
rs137852496
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137852494
rs137852494
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		G 0.800 CausalMutation CLINVAR

dbSNP: rs137852493
rs137852493
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		T 0.800 CausalMutation CLINVAR

dbSNP: rs137852492
rs137852492
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		T 0.800 CausalMutation CLINVAR

dbSNP: rs137852491
rs137852491
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137852490
rs137852490
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		G 0.800 CausalMutation CLINVAR

dbSNP: rs137852487
rs137852487
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137852486
rs137852486
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		G 0.800 CausalMutation CLINVAR

dbSNP: rs137852485
rs137852485
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137852484
rs137852484
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		T 0.800 CausalMutation CLINVAR

dbSNP: rs137852482
rs137852482
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		T 0.800 CausalMutation CLINVAR

dbSNP: rs137852481
rs137852481
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137852480
rs137852480
HPRT1
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		C 0.800 CausalMutation CLINVAR

dbSNP: rs137852479
rs137852479
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		G 0.800 CausalMutation CLINVAR

dbSNP: rs137852478
rs137852478
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		T 0.800 CausalMutation CLINVAR

dbSNP: rs137852477
rs137852477
HPRT1
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related 		G 0.800 CausalMutation CLINVAR