Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02 5
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs10923724 1 119004219 upstream gene variant C/T snv 0.53 3
rs1106529
TBX15
1 118988874 intron variant G/A snv 0.77 3
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 3
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs61823192
LYPLAL1-DT
1 219121228 intron variant C/T snv 1.6E-02 3
rs714515
DNM3 ; PIGC
1 172383850 intron variant G/A snv 0.46 3
rs984222
TBX15
1 118961220 intron variant C/A;G snv 3
rs1044299
PAPPA2
1 176842737 3 prime UTR variant C/G;T snv 2
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 2
rs12042959
SDCCAG8
1 243369971 intron variant A/G;T snv 2
rs17264866
PPIEL
1 39557105 intron variant C/A;G snv 2
rs2061708
COL11A1
1 102951647 intron variant G/A;C;T snv 2
rs2298632
TCEA3
1 23383982 3 prime UTR variant C/T snv 0.40 2