SLC7A9, solute carrier family 7 member 9, 11136

N. diseases: 48; N. variants: 39
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908479
rs121908479
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
T 0.800 CausalMutation CLINVAR
dbSNP: rs121908482
rs121908482
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
T 0.800 CausalMutation CLINVAR
dbSNP: rs121908483
rs121908483
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
T 0.800 CausalMutation CLINVAR
dbSNP: rs121908484
rs121908484
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
A 0.800 CausalMutation CLINVAR
dbSNP: rs121908485
rs121908485
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
G 0.800 CausalMutation CLINVAR
dbSNP: rs121908486
rs121908486
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
A 0.800 CausalMutation CLINVAR
dbSNP: rs121908487
rs121908487
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
C 0.800 CausalMutation CLINVAR
dbSNP: rs79389353
rs79389353
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.800 GeneticVariation UNIPROT
dbSNP: rs1060499787
rs1060499787
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
G 0.700 GeneticVariation CLINVAR
dbSNP: rs142270619
rs142270619
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.700 GeneticVariation UNIPROT
dbSNP: rs766529640
rs766529640
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.700 GeneticVariation UNIPROT
dbSNP: rs768466784
rs768466784
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.700 GeneticVariation UNIPROT
dbSNP: rs774878350
rs774878350
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.700 GeneticVariation UNIPROT
dbSNP: rs939028046
rs939028046
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.700 GeneticVariation UNIPROT
dbSNP: rs964489627
rs964489627
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.700 GeneticVariation UNIPROT
dbSNP: rs7247977
rs7247977
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
T 0.700 GeneticVariation GWASCAT 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. 28452372 2017
dbSNP: rs7247977
rs7247977
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0017654
Disease:
Glomerular Filtration Rate
T 0.700 GeneticVariation GWASCAT 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. 28452372 2017
dbSNP: rs121908479
rs121908479
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.800 GeneticVariation UNIPROT A novel missense mutation of SLC7A9 frequent in Japanese cystinuria cases affecting the C-terminus of the transporter. 16609684 2006
dbSNP: rs121908480
rs121908480
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.800 GeneticVariation UNIPROT A novel missense mutation of SLC7A9 frequent in Japanese cystinuria cases affecting the C-terminus of the transporter. 16609684 2006
dbSNP: rs121908482
rs121908482
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.800 GeneticVariation UNIPROT A novel missense mutation of SLC7A9 frequent in Japanese cystinuria cases affecting the C-terminus of the transporter. 16609684 2006
dbSNP: rs121908483
rs121908483
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.800 GeneticVariation UNIPROT A novel missense mutation of SLC7A9 frequent in Japanese cystinuria cases affecting the C-terminus of the transporter. 16609684 2006
dbSNP: rs121908484
rs121908484
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.800 GeneticVariation UNIPROT A novel missense mutation of SLC7A9 frequent in Japanese cystinuria cases affecting the C-terminus of the transporter. 16609684 2006
dbSNP: rs121908485
rs121908485
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.800 GeneticVariation UNIPROT A novel missense mutation of SLC7A9 frequent in Japanese cystinuria cases affecting the C-terminus of the transporter. 16609684 2006
dbSNP: rs121908486
rs121908486
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.800 GeneticVariation UNIPROT A novel missense mutation of SLC7A9 frequent in Japanese cystinuria cases affecting the C-terminus of the transporter. 16609684 2006
dbSNP: rs121908487
rs121908487
Entrez Id: 11136
Gene Symbol: SLC7A9
SLC7A9
CUI: C0010691
Disease:
Cystinuria
0.800 GeneticVariation UNIPROT A novel missense mutation of SLC7A9 frequent in Japanese cystinuria cases affecting the C-terminus of the transporter. 16609684 2006