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: rs10262915
rs10262915
1 7 94371161 intron variant T/C snv 0.17 0.800 1.000 1 2012 2012
dbSNP: rs10834449
rs10834449
1 11 24718258 intron variant G/A snv 0.56 0.800 1.000 1 2012 2012
dbSNP: rs10995170
rs10995170
1 10 62463624 intron variant T/C snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs11703808
rs11703808
1 22 31628994 intron variant A/G snv 0.49 0.800 1.000 1 2012 2012
dbSNP: rs11713158
rs11713158
1 3 2854000 intron variant T/C snv 0.79 0.800 1.000 1 2012 2012
dbSNP: rs1550404
rs1550404
1 2 126573377 intergenic variant T/G snv 5.1E-02 0.800 1.000 1 2012 2012
dbSNP: rs16835742
rs16835742
1 1 33715242 intron variant G/T snv 8.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs1908039
rs1908039
1 4 130206478 intergenic variant T/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs1987511
rs1987511
1 10 5306374 upstream gene variant T/C snv 0.44 0.800 1.000 1 2012 2012
dbSNP: rs2540051
rs2540051
1 2 200706420 splice donor variant G/A snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs34312136
rs34312136
1 9 134377610 intron variant T/C snv 0.42 0.800 1.000 1 2012 2012
dbSNP: rs3758171
rs3758171
1 9 36997420 intron variant G/A snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs3815908
rs3815908
1 19 48019612 intron variant T/C snv 0.28 0.800 1.000 1 2012 2012
dbSNP: rs5994434
rs5994434
1 22 31833663 intron variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs6043979
rs6043979
1 20 16470997 intron variant A/C;T snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs6781149
rs6781149
1 3 2839891 intron variant A/C;G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs7792596
rs7792596
1 7 94380322 non coding transcript exon variant T/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs1054442
rs1054442
DDN
4 0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 0.700 1.000 4 2017 2019
dbSNP: rs11138902
rs11138902
1 9 69488398 intron variant G/A;T snv 0.700 1.000 4 2017 2019
dbSNP: rs13010010
rs13010010
1 2 100236272 intron variant C/T snv 0.27 0.700 1.000 4 2017 2019
dbSNP: rs17814604
rs17814604
1 6 98137626 intron variant A/G snv 0.19 0.700 1.000 4 2017 2019
dbSNP: rs2239647
rs2239647
7 0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 0.700 1.000 4 2018 2019
dbSNP: rs2251499
rs2251499
2 1.000 0.040 13 105987507 intron variant T/A;C;G snv 0.700 1.000 4 2017 2019
dbSNP: rs34305371
rs34305371
1 1 72267927 intron variant G/A snv 6.6E-02 0.700 1.000 4 2017 2019
dbSNP: rs6801153
rs6801153
2 1.000 0.040 3 24072206 intergenic variant T/C snv 0.74 0.700 1.000 4 2017 2019