SNX17, sorting nexin 17, 9784

N. diseases: 13; N. variants: 5
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: rs4665972
rs4665972
2 27375230 intron variant T/C snv 0.69
CUI: C0001925
Disease: Albuminuria
Albuminuria
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018