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: rs10006235
rs10006235
2 1.000 0.040 4 129748953 non coding transcript exon variant T/C snv 0.73 0.700 1.000 1 2019 2019
dbSNP: rs10010325
rs10010325
4 1.000 0.040 4 105185196 intron variant C/A;G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs10011007
rs10011007
1 4 130143535 intergenic variant A/C snv 8.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs10031823
rs10031823
1 4 102203874 intergenic variant T/C snv 0.68 0.700 1.000 1 2018 2018
dbSNP: rs1003531
rs1003531
1 19 2206576 intron variant G/T snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs10044158
rs10044158
1 5 63666886 intergenic variant G/A snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs10061788
rs10061788
2 1.000 0.040 5 88638889 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10070734
rs10070734
1 5 88644208 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs1007934
rs1007934
3 14 72996771 intron variant G/A snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs1008078
rs1008078
2 1.000 0.040 1 90724174 non coding transcript exon variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10119
rs10119
5 0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs10129426
rs10129426
2 14 103552118 upstream gene variant G/A snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs10133551
rs10133551
1 14 32813026 intron variant T/C snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs10145335
rs10145335
1 14 98081411 intron variant G/A snv 0.21 0.700 1.000 2 2018 2019
dbSNP: rs10147849
rs10147849
1 14 32835225 3 prime UTR variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs10149470
rs10149470
3 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 0.700 1.000 3 2017 2019
dbSNP: rs10165862
rs10165862
1 2 73383615 intron variant C/T snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10175405
rs10175405
1 2 100703250 regulatory region variant G/T snv 0.33 0.700 1.000 1 2017 2017
dbSNP: rs10182272
rs10182272
1 2 165677305 intron variant G/A snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs10185725
rs10185725
1 2 154607197 intergenic variant C/T snv 0.35 0.700 1.000 1 2017 2017
dbSNP: rs10189857
rs10189857
6 1.000 0.080 2 60486100 intron variant A/G snv 0.42 0.700 1.000 2 2018 2019
dbSNP: rs10189912
rs10189912
1 2 143405040 intron variant A/G snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs10191758
rs10191758
1 2 143505711 intron variant A/G snv 0.30 0.700 1.000 2 2017 2017
dbSNP: rs10192369
rs10192369
2 2 160524377 intergenic variant G/A snv 0.45 0.700 1.000 2 2018 2019
dbSNP: rs10193972
rs10193972
1 2 73490529 missense variant A/G snv 0.26 0.39 0.700 1.000 1 2018 2018