Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2284746
rs2284746
2 1 16980180 intron variant C/A;G snv 0.700 1.000 6 2010 2019
dbSNP: rs9435733
rs9435733
3 1 16981759 intron variant T/C snv 0.41 0.700 1.000 1 2017 2017