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: rs1248860
rs1248860
2 1.000 0.040 3 84966628 intron variant G/A snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs2035562
rs2035562
1 3 85007370 intron variant A/G snv 0.74 0.700 1.000 1 2018 2018
dbSNP: rs62253088
rs62253088
1 3 85351651 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs9818122
rs9818122
2 3 85811914 intron variant T/C snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs9852127
rs9852127
2 3 85777586 intron variant G/A snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs9852859
rs9852859
2 3 85793191 intron variant T/C snv 0.15 0.700 1.000 1 2017 2017