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: rs7501939
rs7501939
12 0.776 0.280 17 37741165 intron variant C/T snv 0.41 0.700 1.000 3 2015 2017
dbSNP: rs1508595
rs1508595
5 0.851 0.240 12 88592239 intron variant G/A;T snv 0.700 1.000 2 2013 2013
dbSNP: rs1510272
rs1510272
1 1.000 0.120 3 156582935 regulatory region variant C/T snv 0.25 0.700 1.000 2 2017 2017
dbSNP: rs3782181
rs3782181
4 0.882 0.120 12 88559784 intron variant C/A snv 0.65 0.700 1.000 2 2017 2017
dbSNP: rs7040024
rs7040024
4 0.925 0.120 9 845516 intron variant A/C;G snv 0.700 1.000 2 2017 2017
dbSNP: rs1009647
rs1009647
2 1.000 0.120 14 55413329 upstream gene variant G/A snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs10275045
rs10275045
5 0.882 0.160 7 1881190 intron variant C/T snv 0.35 0.700 1.000 1 2013 2013
dbSNP: rs11071896
rs11071896
2 1.000 0.120 15 66528912 missense variant A/G snv 0.23 0.20 0.700 1.000 1 2017 2017
dbSNP: rs11155671
rs11155671
1 1.000 0.120 6 149650996 upstream gene variant G/A snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs11769858
rs11769858
1 1.000 0.120 7 158708801 upstream gene variant T/C snv 0.60 0.700 1.000 1 2017 2017
dbSNP: rs12481572
rs12481572
1 1.000 0.120 20 52091515 intron variant A/T snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs1267543
rs1267543
1 1.000 0.120 17 58579263 intron variant A/G snv 0.78 0.700 1.000 1 2013 2013
dbSNP: rs12912292
rs12912292
1 1.000 0.120 15 55746509 upstream gene variant G/A snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs17153755
rs17153755
1 1.000 0.120 8 11753991 intron variant C/G snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs17336718
rs17336718
1 1.000 0.120 X 154307767 intron variant C/T snv 4.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs17689040
rs17689040
1 1.000 0.120 7 40880714 intergenic variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2241024
rs2241024
1 1.000 0.120 19 27766485 intron variant G/A snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs2713206
rs2713206
1 1.000 0.120 2 121250365 intron variant C/T snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs34601376
rs34601376
1 1.000 0.120 19 23868026 intron variant A/T snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs3755605
rs3755605
1 1.000 0.120 3 170038331 non coding transcript exon variant C/T snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs3778991
rs3778991
1 1.000 0.120 7 2132820 intron variant G/A snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs3805663
rs3805663
2 1.000 0.120 5 135030510 intron variant A/G snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs4240895
rs4240895
1 1.000 0.120 1 9653328 non coding transcript exon variant C/T snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs4324715
rs4324715
2 0.925 0.160 5 142289942 regulatory region variant C/T snv 0.41 0.700 1.000 1 2013 2013
dbSNP: rs4599029
rs4599029
1 1.000 0.120 19 53781435 intergenic variant G/A;T snv 0.700 1.000 1 2017 2017