Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10045497
rs10045497
5 75340659 intron variant C/A snv 0.35
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2013 2013
dbSNP: rs10045497
rs10045497
5 75340659 intron variant C/A snv 0.35
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2013 2013