SNX17, sorting nexin 17, 9784

N. diseases: 13; N. variants: 5
Disease: Serum albumin measurement ×
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: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012