SNX17, sorting nexin 17, 9784

N. diseases: 13; N. variants: 5
Disease: Triglycerides 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: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 3 2013 2019
dbSNP: rs13472
rs13472 		0.925 0.120 2 27377372 3 prime UTR variant G/A snv 0.38
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1528533
rs1528533 		0.925 0.120 2 27372889 non coding transcript exon variant G/C snv 0.47
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012