rs1263698595
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs181314573
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs28940268
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma.
|
19262603 |
2009 |
rs28940269
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma.
|
19262603 |
2009 |
rs28940270
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma.
|
19262603 |
2009 |
rs28940271
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma.
|
19262603 |
2009 |
rs28940568
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma.
|
19262603 |
2009 |
rs1295935868
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma.
|
19262603 |
2009 |
rs1457513156
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma.
|
19262603 |
2009 |
rs763858530
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma.
|
19262603 |
2009 |
rs28940268
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
|
12915478 |
2003 |
rs28940269
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
|
12915478 |
2003 |
rs28940270
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
|
12915478 |
2003 |
rs28940271
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
|
12915478 |
2003 |
rs28940568
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
|
12915478 |
2003 |
rs1295935868
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
|
12915478 |
2003 |
rs1457513156
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
|
12915478 |
2003 |
rs763858530
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
|
12915478 |
2003 |
rs28940268
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Non-bullous congentital ichthyosiform erythroderma associated with homozygosity for a novel missense mutation in an ATP binding domain of ABCA12.
|
22257947 |
2012 |
rs28940269
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Non-bullous congentital ichthyosiform erythroderma associated with homozygosity for a novel missense mutation in an ATP binding domain of ABCA12.
|
22257947 |
2012 |
rs28940270
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Non-bullous congentital ichthyosiform erythroderma associated with homozygosity for a novel missense mutation in an ATP binding domain of ABCA12.
|
22257947 |
2012 |
rs28940271
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Non-bullous congentital ichthyosiform erythroderma associated with homozygosity for a novel missense mutation in an ATP binding domain of ABCA12.
|
22257947 |
2012 |
rs28940568
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Non-bullous congentital ichthyosiform erythroderma associated with homozygosity for a novel missense mutation in an ATP binding domain of ABCA12.
|
22257947 |
2012 |
rs1295935868
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Non-bullous congentital ichthyosiform erythroderma associated with homozygosity for a novel missense mutation in an ATP binding domain of ABCA12.
|
22257947 |
2012 |
rs1457513156
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Non-bullous congentital ichthyosiform erythroderma associated with homozygosity for a novel missense mutation in an ATP binding domain of ABCA12.
|
22257947 |
2012 |