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: rs10088247
rs10088247
1 1.000 0.040 8 3826677 intron variant C/T snv 0.76 0.700 1.000 1 2010 2010
dbSNP: rs7007032
rs7007032
1 1.000 0.040 8 3821924 intron variant C/T snv 0.75 0.700 1.000 1 2010 2010
dbSNP: rs9987128
rs9987128
1 1.000 0.040 8 3122601 intron variant A/G snv 0.17 0.700 1.000 1 2015 2015