Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894845
rs104894845
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		G 0.860 CausalMutation CLINVAR

dbSNP: rs104894845
rs104894845
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		T 0.860 CausalMutation CLINVAR

dbSNP: rs104894848
rs104894848
GLA ; HNRNPH2 ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		G 0.820 CausalMutation CLINVAR

dbSNP: rs797044613
rs797044613
GLA ; HNRNPH2 ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		G 0.810 CausalMutation CLINVAR

dbSNP: rs28935494
rs28935494
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		G 0.810 CausalMutation CLINVAR

dbSNP: rs28935195
rs28935195
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		T 0.810 CausalMutation CLINVAR

dbSNP: rs104894852
rs104894852
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		C 0.810 CausalMutation CLINVAR

dbSNP: rs869312399
rs869312399
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		C 0.800 CausalMutation CLINVAR

dbSNP: rs869312163
rs869312163
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		T 0.800 GeneticVariation CLINVAR

dbSNP: rs727504348
rs727504348
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		T 0.800 CausalMutation CLINVAR

dbSNP: rs28935495
rs28935495
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		C 0.800 CausalMutation CLINVAR

dbSNP: rs28935492
rs28935492
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		G 0.800 CausalMutation CLINVAR

dbSNP: rs28935491
rs28935491
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		T 0.800 CausalMutation CLINVAR

dbSNP: rs28935489
rs28935489
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		A 0.800 CausalMutation CLINVAR

dbSNP: rs28935488
rs28935488
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		G 0.800 CausalMutation CLINVAR

dbSNP: rs28935487
rs28935487
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		A 0.800 CausalMutation CLINVAR

dbSNP: rs28935196
rs28935196
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		G 0.800 CausalMutation CLINVAR

dbSNP: rs104894838
rs104894838
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		C 0.800 CausalMutation CLINVAR

dbSNP: rs104894837
rs104894837
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		A 0.800 CausalMutation CLINVAR

dbSNP: rs104894836
rs104894836
GLA ; HNRNPH2 ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		C 0.800 CausalMutation CLINVAR

dbSNP: rs104894832
rs104894832
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		T 0.800 CausalMutation CLINVAR

dbSNP: rs727503949
rs727503949
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		A 0.710 CausalMutation CLINVAR

dbSNP: rs398123226
rs398123226
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		T 0.710 CausalMutation CLINVAR

dbSNP: rs104894851
rs104894851
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		T 0.710 CausalMutation CLINVAR

dbSNP: rs879254022
rs879254022
GLA ; RPL36A-HNRNPH2
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		T 0.700 CausalMutation CLINVAR