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: rs2487928
rs2487928
1 1.000 0.040 10 30034963 intron variant G/A snv 0.34 0.710 1.000 3 2015 2018
dbSNP: rs9337951
rs9337951
1 1.000 0.040 10 30028144 synonymous variant G/A snv 0.27 0.25 0.700 1.000 2 2018 2018
dbSNP: rs1887318
rs1887318
1 1.000 0.040 10 30032669 intron variant C/T snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs2505083
rs2505083
3 0.882 0.080 10 30046193 intron variant T/C snv 0.33 0.700 1.000 1 2013 2013