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: rs7759938
rs7759938
7 0.925 0.120 6 104931079 intron variant C/T snv 0.62 0.700 1.000 3 2010 2019
dbSNP: rs9391253
rs9391253
3 6 104919741 intron variant A/T snv 0.29 0.700 1.000 2 2013 2019
dbSNP: rs12207399
rs12207399
1 6 104937737 intron variant G/A snv 0.46 0.700 1.000 1 2019 2019