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: rs1296179669
rs1296179669
2 0.925 0.160 1 11801338 missense variant C/T snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs1383209302
rs1383209302
2 0.925 0.160 13 30756000 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs761740955
rs761740955
FGB
5 0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs1906591
rs1906591
5 0.851 0.200 4 110787733 intergenic variant G/A snv 0.15 0.010 1.000 1 2014 2014
dbSNP: rs2200733
rs2200733
12 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 0.010 1.000 1 2008 2008
dbSNP: rs10033464
rs10033464
8 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1.000 1 2008 2008