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: rs1000778
rs1000778
3 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.010 1.000 1 2017 2017
dbSNP: rs10033464
rs10033464
8 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1.000 1 2017 2017
dbSNP: rs10033601
rs10033601
1 1.000 0.040 4 152330909 intron variant A/G snv 0.37 0.42 0.010 1.000 1 2017 2017
dbSNP: rs1004467
rs1004467
13 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 0.020 1.000 2 2015 2015
dbSNP: rs1004638
rs1004638
3 1.000 0.040 9 22115590 intron variant A/C;T snv 0.010 1.000 1 2009 2009
dbSNP: rs1007888
rs1007888
4 0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46 0.010 1.000 1 2016 2016
dbSNP: rs1008949
rs1008949
1 1.000 0.040 8 22696108 intron variant T/A;C;G snv 0.010 < 0.001 1 2014 2014
dbSNP: rs10093110
rs10093110
1 1.000 0.040 8 105553186 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1010
rs1010
7 0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 0.010 1.000 1 2007 2007
dbSNP: rs10106652
rs10106652
3 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs10116253
rs10116253
4 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 0.010 1.000 1 2017 2017
dbSNP: rs10116277
rs10116277
8 0.827 0.160 9 22081398 intron variant G/T snv 0.62 0.010 1.000 1 2011 2011
dbSNP: rs10118757
rs10118757
7 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.020 1.000 2 2012 2013
dbSNP: rs10128951
rs10128951
1 1.000 0.040 12 124855901 intron variant G/A snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs10131519
rs10131519
1 1.000 0.040 14 99892957 intron variant T/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs10131894
rs10131894
2 1.000 0.040 14 74980176 regulatory region variant C/G snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs10139550
rs10139550
1 1.000 0.040 14 99679373 3 prime UTR variant C/G snv 0.39 0.700 1.000 2 2015 2017
dbSNP: rs10159239
rs10159239
3 0.882 0.040 1 247443750 intron variant G/A snv 0.57 0.010 1.000 1 2020 2020
dbSNP: rs1018383
rs1018383
1 1.000 0.040 6 11784092 intron variant C/T snv 0.76 0.010 1.000 1 2015 2015
dbSNP: rs10186133
rs10186133
1 1.000 0.040 2 113079367 downstream gene variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1020608562
rs1020608562
9 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs10221742
rs10221742
1 1.000 0.040 2 21196778 downstream gene variant G/A snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs10237377
rs10237377
1 1.000 0.040 7 140057336 intron variant G/T snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs1024610
rs1024610
3 0.882 0.200 17 34253212 upstream gene variant T/A snv 0.85 0.020 0.500 2 2015 2019
dbSNP: rs1024611
rs1024611
63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019