SLC22A2, solute carrier family 22 member 2, 6582

N. diseases: 98; N. variants: 16
Disease: Kidney Failure, Chronic ×
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: rs12207180
rs12207180 		1.000 0.080 6 160212075 intron variant T/A;G snv 0.12
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2279463
rs2279463 		1.000 0.080 6 160247357 intron variant A/G;T snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2010 2010