Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs10024899 4 121705035 intergenic variant T/C snv 0.35 1
rs10049088
LINC02029
3 157079859 upstream gene variant C/T snv 0.35 3
rs1006195
HMBS
11 119088159 non coding transcript exon variant G/T snv 0.33 1
rs10065321
SPRY4-AS1
5 142477850 intron variant C/T snv 0.38 1
rs1006705
FLJ12825
12 54065146 intron variant A/G snv 0.66 1
rs10070064 5 173854774 intergenic variant C/T snv 0.26 1
rs1007330
EYA2
20 46897482 intron variant C/T snv 0.33 1
rs10083447
TRIP11
14 91998083 intron variant G/A snv 0.52 1
rs10101067
EYA1
8 71495139 intron variant G/C snv 6.2E-02 2
rs10116353
EPB41L4B
9 109187808 intron variant G/T snv 0.32 1
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10125521
LINC01505
9 106300721 intron variant G/A;C;T snv 1
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10152595
SMAD3
1.000 0.080 15 67183150 intron variant C/G;T snv 2
rs10153926
LOC112268413
2 42961980 intergenic variant G/A snv 0.21 1
rs10164099
KIAA1328
18 37110781 intron variant T/C snv 0.15 1
rs1017698
LOC105373881 ; PNKD
2 218305802 intron variant G/A;C snv 1
rs10177093
CALCRL ; LOC105373786
2 187349092 intron variant G/T snv 0.55 1
rs10190249
LOC105369168
2 66015391 intron variant G/A snv 0.24 1
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs10245353 7 25818994 intergenic variant C/A snv 0.16 3
rs10260148
LOC105375508
1.000 0.080 7 130746210 intergenic variant C/T snv 0.27 2
rs10264590
RSBN1L
7 77728431 intron variant A/G snv 0.58 1