LAMA2, laminin subunit alpha 2, 3908

N. diseases: 167; N. variants: 127
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913570
rs121913570
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		C 0.800 CausalMutation CLINVAR
dbSNP: rs147077184
rs147077184
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C4748327
Disease:
MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23 		T 0.800 CausalMutation CLINVAR
dbSNP: rs886039896
rs886039896
Entrez Id: 3908;102723409
Gene Symbol: LAMA2;LOC102723409
LAMA2;LOC102723409
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		A 0.800 CausalMutation CLINVAR
dbSNP: rs1055407857
rs1055407857
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1064797040
rs1064797040
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1064797327
rs1064797327
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1131691660
rs1131691660
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1131691660
rs1131691660
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs117422805
rs117422805
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		0.700 GeneticVariation UNIPROT
dbSNP: rs1209130981
rs1209130981
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs121913569
rs121913569
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121913572
rs121913572
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C4748327
Disease:
MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121913574
rs121913574
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1842898
Disease:
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121913575
rs121913575
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1842898
Disease:
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121913576
rs121913576
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1842898
Disease:
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121913577
rs121913577
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1246940477
rs1246940477
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1262029350
rs1262029350
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1262029350
rs1262029350
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1278823424
rs1278823424
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1289855948
rs1289855948
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1296761337
rs1296761337
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1326401124
rs1326401124
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1360796756
rs1360796756
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1374568851
rs1374568851
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C1263858
Disease:
Muscular dystrophy congenital, merosin negative 		T 0.700 GeneticVariation CLINVAR