Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886042086
rs886042086
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.800 GeneticVariation UNIPROT

dbSNP: rs757111744
rs757111744
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.800 GeneticVariation UNIPROT

dbSNP: rs730880022
rs730880022
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		A 0.800 CausalMutation CLINVAR

dbSNP: rs374143224
rs374143224
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.800 GeneticVariation UNIPROT

dbSNP: rs121907940
rs121907940
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		C 0.800 CausalMutation CLINVAR

dbSNP: rs996798292
rs996798292
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		CTGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs886043920
rs886043920
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886043920
rs886043920
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs886043343
rs886043343
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs786204646
rs786204646
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		C 0.700 CausalMutation CLINVAR

dbSNP: rs786204549
rs786204549
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		T 0.700 CausalMutation CLINVAR

dbSNP: rs780321415
rs780321415
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		T 0.700 CausalMutation CLINVAR

dbSNP: rs777275355
rs777275355
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs775450536
rs775450536
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.700 GeneticVariation UNIPROT

dbSNP: rs773417785
rs773417785
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.700 GeneticVariation UNIPROT

dbSNP: rs772962666
rs772962666
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.700 GeneticVariation UNIPROT

dbSNP: rs761317813
rs761317813
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs756024023
rs756024023
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs730880372
rs730880372
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		CA 0.700 CausalMutation CLINVAR

dbSNP: rs374470794
rs374470794
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.700 GeneticVariation UNIPROT

dbSNP: rs200210219
rs200210219
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.700 GeneticVariation UNIPROT

dbSNP: rs1567835781
rs1567835781
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1567835775
rs1567835775
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555603434
rs1555603434
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555603318
rs1555603318
GAA
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		A 0.700 GeneticVariation CLINVAR