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: rs2242652
rs2242652
16 0.724 0.400 5 1279913 intron variant G/A snv 0.18 0.710 1.000 3 2011 2018
dbSNP: rs7725218
rs7725218
17 0.708 0.280 5 1282299 intron variant G/A snv 0.38 0.700 1.000 2 2015 2016
dbSNP: rs2736100
rs2736100
83 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 0.020 1.000 2 2015 2015
dbSNP: rs7726159
rs7726159
10 0.790 0.160 5 1282204 intron variant C/A snv 0.29 0.020 1.000 2 2015 2015
dbSNP: rs10069690
rs10069690
53 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015
dbSNP: rs2736098
rs2736098
48 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 0.010 1.000 1 2015 2015
dbSNP: rs2853669
rs2853669
35 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 0.010 1.000 1 2015 2015