Disease: Intelligence
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 7
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 6
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42 4
rs10752262
CAMK1D
1.000 0.040 10 12353101 intron variant C/T snv 0.39 3
rs11765189
PTPRN2
1.000 0.040 7 157743285 intron variant A/G snv 0.25 3
rs12602286
EPN2
1.000 0.040 17 19333641 intron variant G/T snv 0.79 3
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs3747631
LOC105371692 ; LRRN2
1.000 0.040 1 204618441 missense variant G/A;C snv 4.0E-06; 0.20 3
rs4396807
TRIOBP
22 37742372 intron variant G/C snv 0.38 3
rs62154720
TGFBRAP1
1.000 0.040 2 105306623 intron variant C/T snv 9.2E-02 3
rs6731373
LOC107985892
2 68275912 intergenic variant G/A snv 0.29 3
rs7581162
BCL11A
2 60477349 intron variant T/A snv 0.49 3
rs76076331
PDIA6
1.000 0.040 2 10837459 intron variant C/T snv 1.0E-01 3
rs7963801
SYT1
12 79291446 intron variant T/C snv 0.70 3
rs9556958
FARP1 ; STK24
1.000 0.040 13 98447792 3 prime UTR variant C/G;T snv 3
rs9616914
SHANK3
1.000 0.040 22 50678709 intron variant G/A snv 0.35 0.36 3
rs10129426 14 103552118 upstream gene variant G/A snv 0.54 2
rs10192369 2 160524377 intergenic variant G/A snv 0.45 2
rs10783018
LOC101928219 ; LINC02607
1 95782279 non coding transcript exon variant G/A snv 0.74 2
rs10922907 1 90727492 downstream gene variant A/G;T snv 2
rs10949662
PTPRN2
7 157741413 intron variant C/A;T snv 2