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: rs1016883
rs1016883
1 1.000 0.040 2 198016944 intron variant G/A snv 0.20 0.800 1.000 1 2012 2012
dbSNP: rs1440088
rs1440088
1 1.000 0.040 2 198006693 intron variant T/G snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs1595825
rs1595825
1 1.000 0.040 2 198010740 intron variant G/A snv 0.23 0.700 1.000 1 2015 2015