Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44 6
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46 5
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs34338164
PLEK
2 68388414 missense variant A/C snv 8.0E-03 7.8E-03 4
rs3812049
SLC12A2 ; LINC01184
5 128083158 non coding transcript exon variant C/A;G;T snv 4
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs13092376
PAK2
3 196789417 intron variant A/C;G snv 0.33 3
rs149290349
ZFP36L2
2 43224818 missense variant G/A;T snv 6.7E-02 3
rs28577594
RILPL2
12 123411359 3 prime UTR variant G/C snv 0.56 3
rs36084354
ARHGAP45
19 1079960 missense variant G/A snv 5.7E-02 5.9E-02 3
rs61387190
SMG9
19 43756777 upstream gene variant C/A;T snv 3
rs62237617
TTC28
22 28365160 intron variant C/G;T snv 1.9E-03 3
rs748113
VSIR ; CDH23
10 71749034 3 prime UTR variant T/C snv 0.38 3
rs79716587
ARHGAP15
2 143129250 intron variant G/A snv 7.9E-02 3
rs9494142
LOC105378010
6 135110502 TF binding site variant T/C snv 0.21 3
rs10087240
PVT1
8 128000328 intron variant C/G;T snv 2
rs10422126
MIR24-2 ; MIR27A ; MIR23A ; LOC284454
19 13837498 non coding transcript exon variant G/A snv 0.37 2
rs1285886
RREB1
6 7140598 intron variant G/A snv 0.28 2
rs17041439
SPIC
12 101479462 intron variant A/C snv 7.0E-02 2
rs175714
LOC105370572
14 75515513 TF binding site variant T/C snv 0.50 2