LMOD3, leiomodin 3, 56203

N. diseases: 67; N. variants: 8
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1274699363
rs1274699363
Entrez Id: 56203
Gene Symbol: LMOD3
LMOD3
CUI: C4015360
Disease:
NEMALINE MYOPATHY 10
G 0.700 CausalMutation CLINVAR
dbSNP: rs1368453406
rs1368453406
Entrez Id: 56203
Gene Symbol: LMOD3
LMOD3
CUI: C4015360
Disease:
NEMALINE MYOPATHY 10
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1426709672
rs1426709672
Entrez Id: 56203
Gene Symbol: LMOD3
LMOD3
CUI: C4015360
Disease:
NEMALINE MYOPATHY 10
T 0.700 CausalMutation CLINVAR
dbSNP: rs724159964
rs724159964
Entrez Id: 56203
Gene Symbol: LMOD3
LMOD3
CUI: C4015360
Disease:
NEMALINE MYOPATHY 10
A 0.700 CausalMutation CLINVAR
dbSNP: rs724159965
rs724159965
Entrez Id: 56203
Gene Symbol: LMOD3
LMOD3
CUI: C4015360
Disease:
NEMALINE MYOPATHY 10
A 0.700 CausalMutation CLINVAR
dbSNP: rs727502797
rs727502797
Entrez Id: 56203
Gene Symbol: LMOD3
LMOD3
CUI: C4015360
Disease:
NEMALINE MYOPATHY 10
TG 0.700 CausalMutation CLINVAR
dbSNP: rs727502798
rs727502798
Entrez Id: 56203
Gene Symbol: LMOD3
LMOD3
CUI: C4015360
Disease:
NEMALINE MYOPATHY 10
G 0.700 CausalMutation CLINVAR
dbSNP: rs727502799
rs727502799
Entrez Id: 56203
Gene Symbol: LMOD3
LMOD3
CUI: C4015360
Disease:
NEMALINE MYOPATHY 10
G 0.700 CausalMutation CLINVAR