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: rs10031466
rs10031466
2 4 188094248 intron variant G/A snv 0.56 0.700 1.000 1 2015 2015
dbSNP: rs1003858
rs1003858
2 9 116202676 intron variant G/C snv 1.1E-02 0.700 1.000 1 2015 2015
dbSNP: rs10041657
rs10041657
FER
2 5 108816727 intron variant G/A snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs1013443
rs1013443
1 5 180774114 intergenic variant A/T snv 1.4E-03 0.700 1.000 1 2012 2012
dbSNP: rs1014242
rs1014242
1 7 32232693 intron variant C/T snv 0.54 0.700 1.000 1 2010 2010
dbSNP: rs1014667
rs1014667
2 2 50521617 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs10195252
rs10195252
7 0.925 0.080 2 164656581 intron variant T/C snv 0.48 0.700 1.000 1 2017 2017
dbSNP: rs1021070
rs1021070
1 15 78654521 intron variant C/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs1021071
rs1021071
3 15 78675837 intron variant G/C snv 0.28 0.700 1.000 2 2010 2010
dbSNP: rs10226228
rs10226228
1 7 32276001 intron variant A/G snv 0.38 0.700 1.000 1 2010 2010
dbSNP: rs10236197
rs10236197
2 7 32252149 intron variant T/C snv 0.41 0.700 1.000 1 2010 2010
dbSNP: rs10245353
rs10245353
4 7 25818994 intergenic variant C/A snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs10259431
rs10259431
1 7 32241785 intron variant C/T snv 0.54 0.700 1.000 1 2010 2010
dbSNP: rs10264177
rs10264177
1 7 32331250 intron variant A/G snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs10269774
rs10269774
2 7 92624658 intron variant G/A snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs1028936
rs1028936
1 10 91590040 regulatory region variant A/C snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs10425738
rs10425738
2 19 40911822 non coding transcript exon variant G/A snv 0.74 0.700 1.000 1 2016 2016
dbSNP: rs10440708
rs10440708
2 5 173223484 downstream gene variant A/G snv 4.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs1045241
rs1045241
6 1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs10488693
rs10488693
2 11 61717684 intron variant C/T snv 6.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs1049281
rs1049281
3 1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs10501157
rs10501157
2 11 36485319 3 prime UTR variant T/C snv 1.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs10503023
rs10503023
2 18 59165543 intergenic variant G/A snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs10508503
rs10508503
2 1.000 0.080 10 16257952 intergenic variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs1051730
rs1051730
43 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 0.700 1.000 4 2010 2012