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: rs77944304
rs77944304
1 1 72117096 intron variant C/T snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs9424976
rs9424976
1 1 72252927 intron variant T/C;G snv 0.700 1.000 1 2018 2018