Gene: LMNA ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs58932704
rs58932704
LMNA
T 0.810 CausalMutation CLINVAR

dbSNP: rs57520892
rs57520892
LMNA
C 0.800 CausalMutation CLINVAR

dbSNP: rs60934003
rs60934003
LMNA
C 0.800 CausalMutation CLINVAR

dbSNP: rs28933091
rs28933091
LMNA
G 0.710 CausalMutation CLINVAR

dbSNP: rs61672878
rs61672878
LMNA
A 0.710 CausalMutation CLINVAR

dbSNP: rs11575937
rs11575937
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553265999
rs1553265999
LMNA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs267607539
rs267607539
LMNA
C 0.700 CausalMutation CLINVAR

dbSNP: rs267607540
rs267607540
LMNA
C 0.700 CausalMutation CLINVAR

dbSNP: rs267607632
rs267607632
LMNA
C 0.700 CausalMutation CLINVAR

dbSNP: rs386134243
rs386134243
LMNA
T 0.700 CausalMutation CLINVAR

dbSNP: rs56699480
rs56699480
LMNA
T 0.700 CausalMutation CLINVAR

dbSNP: rs56771886
rs56771886
LMNA
C 0.700 CausalMutation CLINVAR

dbSNP: rs58048078
rs58048078
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs60458016
rs60458016
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs60682848
rs60682848
LMNA
T 0.700 CausalMutation CLINVAR

dbSNP: rs61046466
rs61046466
LMNA
T 0.700 CausalMutation CLINVAR

dbSNP: rs61195471
rs61195471
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs61295588
rs61295588
LMNA
C 0.700 CausalMutation CLINVAR

dbSNP: rs57629361
rs57629361
LMNA
A 0.800 GeneticVariation CLINVAR In situ hybridization detection of HTLV-I RNA in peripheral blood mononuclear cells of TSP/HAM patients and their spouses. 1849984

1991
dbSNP: rs57629361
rs57629361
LMNA
A 0.800 GeneticVariation CLINVAR Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy. 10739764

2000
dbSNP: rs59332535
rs59332535
LMNA
A 0.700 CausalMutation CLINVAR Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy. 10739764

2000
dbSNP: rs57207746
rs57207746
LMNA
A 0.800 GeneticVariation CLINVAR Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene. 10939567

2000
dbSNP: rs57629361
rs57629361
LMNA
A 0.800 GeneticVariation CLINVAR Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene. 10939567

2000
dbSNP: rs59332535
rs59332535
LMNA
A 0.700 CausalMutation CLINVAR Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene. 10939567

2000