Disease: Intelligence
Source: GWASCAT ×
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 24
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs12764899
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875346 intron variant G/A snv 0.21 4
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 4
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs7599488
BCL11A
0.925 0.120 2 60491212 intron variant C/T snv 0.42 4
rs10752262
CAMK1D
1.000 0.040 10 12353101 intron variant C/T snv 0.39 3
rs11688767
ACTG1P22
0.925 0.040 2 57761059 intron variant A/T snv 0.40 3
rs11740474
GALNT10
1.000 0.040 5 154301187 intron variant A/T snv 0.37 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
rs12704290
GRM3-AS1 ; GRM3
1.000 0.040 7 86798310 intron variant G/A snv 8.9E-02 3
rs12826178
SHMT2
1.000 0.040 12 57228588 upstream gene variant G/T snv 5.3E-02 3
rs133047
MRTFA
1.000 0.040 22 40631815 intron variant T/C snv 0.93 3
rs1408579
ERLIN1
1.000 0.040 10 100152437 intron variant C/T snv 0.32 3
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 3
rs268134
SPRED2
0.925 0.120 2 65381229 intron variant A/C;G;T snv 3
rs28600726 1.000 0.040 4 158730723 intergenic variant G/A snv 0.53 3
rs28669908
CHRNA3
1.000 0.040 15 78617925 intron variant C/A snv 0.18 3