Source: GWASDB

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: rs28385681
rs28385681
2 102017062 intron variant T/G snv 1.4E-05
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs4321386
rs4321386
2 101996551 intron variant C/G snv 0.12
Follicle stimulating hormone measurement
0.700 1.000 1 2013 2013