Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9994759
rs9994759
4 31891570 intergenic variant T/C snv 0.23
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9993636
rs9993636
4 27977139 intron variant C/T snv 0.83
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9986272
rs9986272
5 88824509 intron variant C/T snv 4.4E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9977825
rs9977825
21 45075080 intron variant T/C;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9964831
rs9964831
18 39827726 intergenic variant C/T snv 0.69
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9959497
rs9959497
18 1851687 intron variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9957365
rs9957365
18 25072853 intron variant A/G snv 0.28
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9938394
rs9938394
16 28235347 downstream gene variant C/T snv 0.60
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9934011
rs9934011
16 13821950 intergenic variant T/C snv 0.21
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9933476
rs9933476
16 83353192 intron variant G/A snv 0.57
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9933256
rs9933256
16 1196748 intron variant A/G snv 0.43
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9932312
rs9932312
16 90049151 upstream gene variant A/G snv 0.63
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9927295
rs9927295
16 31066088 intron variant A/G snv 0.76
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9915356
rs9915356
17 33285476 intron variant A/G;T snv 0.50
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9906951
rs9906951
17 39891991 intergenic variant T/C snv 0.46
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9891111
rs9891111
17 47632009 intron variant C/A;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9889827
rs9889827
17 78030590 intron variant T/C snv 0.47
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9886703
rs9886703
9 79631436 intron variant A/T snv 0.79
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9883813
rs9883813
3 49333111 intron variant C/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs987773
rs987773
6 99154010 intergenic variant C/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9877235
rs9877235
3 110545413 intergenic variant T/G snv 0.59
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9877137
rs9877137
3 94328528 intergenic variant T/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9874646
rs9874646
3 62477143 intron variant C/T snv 0.73
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9872276
rs9872276
3 41190477 upstream gene variant C/T snv 0.40
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9869493
rs9869493
3 82528124 intergenic variant T/A snv 0.20
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018