Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs227283
MANBA
0.925 0.120 4 102686096 intron variant C/G;T snv 2
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 2
rs1592757 1.000 0.040 5 104554297 intron variant G/C snv 0.29 1
rs325485
LOC105379109
0.925 0.120 5 104659667 intron variant A/G snv 0.65 2
rs11591402
SORCS3
1.000 0.040 10 104987596 intron variant T/A;G snv 1
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs11074889
EMP2
1.000 0.040 16 10539308 intron variant A/G;T snv 1
rs6539247
NUAK1
1.000 0.040 12 106066124 3 prime UTR variant T/C;G snv 1
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs10492664 0.925 0.040 13 108163877 intergenic variant C/A;T snv 2
rs2341917
ACOXL
1.000 0.040 2 110953512 intron variant A/G snv 0.12 1
rs1476535
FOXP2
0.925 0.040 7 114430980 intron variant C/G;T snv 2
rs5886709
FOXP2
1.000 0.040 7 114446079 intron variant CT/- delins 0.39 1
rs2189012
FOXP2
0.925 0.040 7 114571857 intron variant G/A snv 0.73 2
rs7089973
TAF9BP2 ; ABLIM1
0.925 0.040 10 114809806 intron variant C/A snv 0.41 2
rs968847 0.925 0.040 10 114998320 downstream gene variant G/T snv 0.20 2
rs10983238
LOC107987015 ; ASTN2
1.000 0.040 9 116571404 intron variant C/A;G snv 0.16 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs1334489 0.925 0.040 6 118318224 downstream gene variant T/A snv 0.37 2
rs12661338
CEP85L ; LOC105377971
0.925 0.040 6 118473527 intron variant C/A snv 0.35 2
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 2
rs11756438
CEP85L
0.925 0.040 6 118672469 intron variant C/A snv 0.42 3