Gene: SMG7 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs119103274
rs119103274
NCF2 ; SMG7
A 0.700 CausalMutation CLINVAR

dbSNP: rs119103275
rs119103275
NCF2 ; SMG7
T 0.700 CausalMutation CLINVAR

dbSNP: rs119103276
rs119103276
NCF2 ; SMG7
A 0.700 CausalMutation CLINVAR

dbSNP: rs1290169467
rs1290169467
NCF2 ; SMG7
A 0.700 CausalMutation CLINVAR

dbSNP: rs1558098982
rs1558098982
NCF2 ; SMG7
C 0.700 CausalMutation CLINVAR

dbSNP: rs374402066
rs374402066
NCF2 ; SMG7
A 0.700 CausalMutation CLINVAR

dbSNP: rs777621636
rs777621636
NCF2 ; SMG7
T 0.700 CausalMutation CLINVAR

dbSNP: rs796065030
rs796065030
NCF2 ; SMG7
TTC 0.700 CausalMutation CLINVAR

dbSNP: rs796065031
rs796065031
NCF2 ; SMG7
C 0.700 CausalMutation CLINVAR

dbSNP: rs796065032
rs796065032
NCF2 ; SMG7
T 0.700 CausalMutation CLINVAR

dbSNP: rs796065033
rs796065033
NCF2 ; SMG7
A 0.700 CausalMutation CLINVAR

dbSNP: rs137854508
rs137854508
NCF2 ; SMG7
0.800 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854507
rs137854507
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854509
rs137854509
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854510
rs137854510
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854514
rs137854514
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854515
rs137854515
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854516
rs137854516
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854517
rs137854517
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854518
rs137854518
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854519
rs137854519
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854520
rs137854520
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs796065033
rs796065033
NCF2 ; SMG7
A 0.700 GeneticVariation CLINVAR Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813

1999
dbSNP: rs137854508
rs137854508
NCF2 ; SMG7
0.800 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component: identification of mutation and detection of carriers. 8286749

1994
dbSNP: rs137854507
rs137854507
NCF2 ; SMG7
0.700 GeneticVariation UNIPROT Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component: identification of mutation and detection of carriers. 8286749

1994