PEX10, peroxisomal biogenesis factor 10, 5192

N. diseases: 141; N. variants: 27
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61752095
rs61752095
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
C 0.800 CausalMutation CLINVAR
dbSNP: rs1335685844
rs1335685844
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1335685844
rs1335685844
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1335685844
rs1335685844
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1335685844
rs1335685844
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1553231739
rs1553231739
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1553231739
rs1553231739
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1553231739
rs1553231739
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1553231739
rs1553231739
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1553231875
rs1553231875
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1553231875
rs1553231875
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1553231888
rs1553231888
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
GAG 0.700 GeneticVariation CLINVAR
dbSNP: rs1553231888
rs1553231888
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
GAG 0.700 GeneticVariation CLINVAR
dbSNP: rs1553231896
rs1553231896
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1553231896
rs1553231896
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1553232077
rs1553232077
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1553232077
rs1553232077
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1553232917
rs1553232917
Entrez Id: 5192;9651
Gene Symbol: PEX10;PLCH2
PEX10;PLCH2
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1553232917
rs1553232917
Entrez Id: 5192;9651
Gene Symbol: PEX10;PLCH2
PEX10;PLCH2
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1553232926
rs1553232926
Entrez Id: 5192;9651
Gene Symbol: PEX10;PLCH2
PEX10;PLCH2
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1553232926
rs1553232926
Entrez Id: 5192;9651
Gene Symbol: PEX10;PLCH2
PEX10;PLCH2
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
G 0.700 GeneticVariation CLINVAR
dbSNP: rs267608183
rs267608183
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553947
Disease:
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)
T 0.700 CausalMutation CLINVAR
dbSNP: rs61750434
rs61750434
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
A 0.700 CausalMutation CLINVAR
dbSNP: rs724159999
rs724159999
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
A 0.700 CausalMutation CLINVAR
dbSNP: rs768893724
rs768893724
Entrez Id: 5192
Gene Symbol: PEX10
PEX10
CUI: C3553948
Disease:
PEROXISOME BIOGENESIS DISORDER 6B
T 0.700 GeneticVariation CLINVAR