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: rs4348675
rs4348675
1 1 72050034 intron variant T/C snv 9.0E-02 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