Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1864325
MAPT
0.882 0.160 17 45900461 intron variant C/T snv 0.14 5
rs3130340
TSBP1-AS1
0.851 0.200 6 32276850 intron variant T/C snv 0.25 4
rs10876432
SP7
12 53338107 intron variant G/A snv 2
rs12407028
GNG12-AS1 ; WLS
1 68182033 intron variant T/A;C snv 0.35 2
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 2
rs1430740
GNG12-AS1 ; WLS
1 68191827 intron variant T/C snv 0.58 2
rs2016266
SP7
1.000 0.080 12 53334171 intron variant G/A;C snv 2
rs2062305
LINC02341
1.000 0.040 13 42478744 intron variant G/A snv 0.46 2
rs2504063
LOC107986529 ; ESR1
6 151769572 intron variant A/G snv 0.50 2
rs4424296
COLEC10
8 119001037 intron variant C/T snv 0.61 2
rs4727338
SEM1 ; LOC105375411
7 96491363 intron variant G/C;T snv 2
rs4869742
CCDC170
6 151586613 intron variant C/A;G;T snv 2
rs6909279
CCDC170
6 151574321 intron variant G/C;T snv 2
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs9533090
LINC02341
13 42377313 intron variant C/T snv 0.39 2
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv 1
rs1007738
CKAP5
11 46827809 intron variant G/A snv 0.64 1
rs10085588
LOC105375412 ; SEM1 ; LOC105375411
1.000 0.080 7 96508362 intron variant A/G snv 0.72 1
rs10086835
COLEC10
8 119027942 intron variant C/T snv 0.63 1
rs10091277
COLEC10
8 119022148 intron variant A/G snv 0.53 1
rs10098408
COLEC10
8 119027482 intron variant T/C snv 0.58 1
rs10226308
EPDR1 ; NME8
7 37898820 intron variant A/C;G snv 1
rs1023940
LOC107986528 ; CCDC170
6 151611643 intron variant A/G snv 0.58 1
rs1036066
GNG12-AS1 ; WLS
1 68194522 intron variant A/C snv 0.33 1
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58 1