Source: GWASCAT

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: rs10006237
rs10006237
4 136606920 intergenic variant C/T snv 0.50
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10009397
rs10009397
4 28695228 intergenic variant A/T snv 0.89
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10009715
rs10009715
4 171510209 intron variant T/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10026457
rs10026457
4 58384912 intergenic variant T/G snv 0.71
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10040865
rs10040865
5 171411280 downstream gene variant G/A snv 0.40
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10055216
rs10055216
5 170981562 intron variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10057590
rs10057590
5 124999554 intron variant A/C snv 0.62
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10061387
rs10061387
5 124524355 intron variant A/G snv 0.47
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10064431
rs10064431
5 93614967 downstream gene variant T/C snv 0.41
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10065159
rs10065159
5 172668864 intron variant T/C snv 0.77
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10066711
rs10066711
5 88894787 intron variant A/T snv 0.52
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10073038
rs10073038
5 111230823 intron variant A/T snv 0.38
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs1007966
rs1007966
9 89599052 non coding transcript exon variant G/A snv 0.50
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10088255
rs10088255
8 102355371 intron variant A/T snv 0.55
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10098073
rs10098073
1.000 0.040 8 142228143 intron variant C/A snv 0.35
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10106406
rs10106406
8 140996099 intron variant C/A;G snv 0.45
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10107533
rs10107533
8 19521910 intron variant C/A;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10109012
rs10109012
8 15387338 intergenic variant C/T snv 0.52
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs1011392
rs1011392
18 55374672 intron variant A/G snv 0.39
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10114066
rs10114066
9 73908824 intergenic variant T/A snv 0.76
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10122976
rs10122976
9 135751066 intron variant C/A;T snv 0.47; 1.2E-05
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10129426
rs10129426
14 103552118 upstream gene variant G/A snv 0.54
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10132779
rs10132779
14 29249690 intron variant A/G snv 0.19
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10136545
rs10136545
14 54886145 non coding transcript exon variant C/T snv 0.41
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10137343
rs10137343
14 22913431 intron variant A/T snv 0.56
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018