KLHL41, kelch like family member 41, 10324

N. diseases: 94; N. variants: 7
Disease: NEMALINE MYOPATHY 9 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1247404453
rs1247404453
Entrez Id: 10324
Gene Symbol: KLHL41
KLHL41
CUI: C3810384
Disease:
NEMALINE MYOPATHY 9 		G 0.700 CausalMutation CLINVAR
dbSNP: rs730882235
rs730882235
Entrez Id: 10324
Gene Symbol: KLHL41
KLHL41
CUI: C3810384
Disease:
NEMALINE MYOPATHY 9 		T 0.700 CausalMutation CLINVAR
dbSNP: rs730882257
rs730882257
Entrez Id: 10324
Gene Symbol: KLHL41
KLHL41
CUI: C3810384
Disease:
NEMALINE MYOPATHY 9 		ACTC 0.700 CausalMutation CLINVAR
dbSNP: rs730882258
rs730882258
Entrez Id: 10324
Gene Symbol: KLHL41
KLHL41
CUI: C3810384
Disease:
NEMALINE MYOPATHY 9 		G 0.700 CausalMutation CLINVAR
dbSNP: rs730882259
rs730882259
Entrez Id: 10324
Gene Symbol: KLHL41
KLHL41
CUI: C3810384
Disease:
NEMALINE MYOPATHY 9 		A 0.700 CausalMutation CLINVAR
dbSNP: rs730882260
rs730882260
Entrez Id: 10324
Gene Symbol: KLHL41
KLHL41
CUI: C3810384
Disease:
NEMALINE MYOPATHY 9 		T 0.700 CausalMutation CLINVAR
dbSNP: rs775513051
rs775513051
Entrez Id: 10324
Gene Symbol: KLHL41
KLHL41
CUI: C3810384
Disease:
NEMALINE MYOPATHY 9 		GA 0.700 CausalMutation CLINVAR