SLC7A9, solute carrier family 7 member 9, 11136

N. diseases: 48; N. variants: 39
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7247977
rs7247977
19 32867449 intron variant T/C snv 0.46
Creatinine measurement, serum (procedure)
0.700 1.000 2 2017 2018
dbSNP: rs7247977
rs7247977
19 32867449 intron variant T/C snv 0.46
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 2 2017 2019
dbSNP: rs10421876
rs10421876
19 32871878 upstream gene variant C/T snv 0.36
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs2868194
rs2868194
19 32859154 intron variant T/C snv 0.63
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs121908479
rs121908479
0.925 0.120 19 32862557 missense variant C/T snv 4.0E-06
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.800 1.000 11 1999 2012
dbSNP: rs121908479
rs121908479
0.925 0.120 19 32862557 missense variant C/T snv 4.0E-06
CUI: C0268643
Disease: Cystinuria type 1
Cystinuria type 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2000 2000
dbSNP: rs121908480
rs121908480
1.000 0.120 19 32864261 missense variant C/T snv 2.7E-04 1.7E-04
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.800 1.000 14 1999 2015
dbSNP: rs121908482
rs121908482
1.000 0.120 19 32862482 missense variant C/T snv 8.0E-06
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.800 1.000 11 1999 2012
dbSNP: rs121908484
rs121908484
1.000 0.120 19 32843932 missense variant G/A snv 8.8E-05 4.2E-05
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.800 1.000 11 1999 2012
dbSNP: rs121908485
rs121908485
1.000 0.120 19 32864733 missense variant A/G snv
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.800 1.000 11 1999 2012
dbSNP: rs121908486
rs121908486
1.000 0.120 19 32859932 missense variant G/A snv 1.1E-04 1.4E-04
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.800 1.000 11 1999 2012
dbSNP: rs121908487
rs121908487
1.000 0.120 19 32862127 missense variant T/C snv 1.1E-04 1.2E-04
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.800 1.000 11 1999 2012
dbSNP: rs1198613438
rs1198613438
1.000 0.120 19 32864709 missense variant G/A snv 4.0E-06
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs121908483
rs121908483
1.000 0.120 19 32859939 missense variant C/T snv 8.0E-06 7.0E-06
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.800 1.000 10 1999 2010
dbSNP: rs1357600282
rs1357600282
1.000 0.120 19 32859867 missense variant G/A snv 7.0E-06
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs1395997436
rs1395997436
1.000 0.120 19 32864677 missense variant C/T snv
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs146815072
rs146815072
1.000 0.120 19 32830639 missense variant G/A snv 3.6E-05 4.9E-05
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs368441237
rs368441237
1.000 0.120 19 32862506 missense variant T/A snv 3.2E-05 4.2E-05
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs372306844
rs372306844
1.000 0.120 19 32864198 missense variant C/T snv 2.0E-05 3.5E-05
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs531029519
rs531029519
1.000 0.120 19 32862503 missense variant C/G;T snv 4.0E-06; 2.4E-05
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs755135545
rs755135545
1.000 0.120 19 32859857 missense variant G/A snv 4.0E-06
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs760264924
rs760264924
1.000 0.120 19 32842191 missense variant T/C snv 1.2E-05 7.0E-06
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs769448665
rs769448665
1.000 0.120 19 32864655 missense variant G/A snv 2.0E-05 7.0E-06
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs769576205
rs769576205
1.000 0.120 19 32843931 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010
dbSNP: rs777371504
rs777371504
1.000 0.120 19 32860633 missense variant A/G snv 4.0E-06
CUI: C0010691
Disease: Cystinuria
Cystinuria
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 10 1999 2010