Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs36053385
FAM53B
10 124720306 intron variant -/A delins 0.61 1
rs11442179
ARG1
6 131553246 intron variant -/C delins 0.33 1
rs375125008 11 65739571 regulatory region variant -/CCTTTTT;CTTTTT;CTTTTTTCTTTTT delins 0.26 1
rs55951234
PLA2G6 ; MAFF
22 38205423 5 prime UTR variant -/CTC delins 2
rs149165215
GGT7
20 34846312 intron variant -/CTTTCTTTT;CTTTT;CTTTTT delins 1
rs200210321
SUGP1
19 19283081 intron variant -/G ins 5.9E-02 1
rs35505876
DYDC2
10 80363511 intron variant -/G;GT;GTT;GTTT;GTTTT ins 1
rs35870583 20 54118699 regulatory region variant -/T;TT delins 1
rs140582693
EYA4
6 133478448 intron variant -/TA;TATA delins 1
rs10687766
RAI1
17 17688488 intron variant -/TAATAA delins 1
rs112578436
C2orf73
2 54344716 intron variant -/TGTC delins 1
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 4
rs491567
WDR72
1.000 0.080 15 53654396 intron variant A/C snv 0.34 3
rs143297173 6 55418058 intergenic variant A/C snv 6.7E-04 2
rs2490391
SDCCAG8
1.000 0.080 1 243306367 3 prime UTR variant A/C snv 0.50 2
rs1031755
WDR72
15 53659238 intron variant A/C snv 0.22 1
rs10846157
RERG
12 15172097 intron variant A/C snv 0.29 1
rs113401767 X 8942922 intergenic variant A/C snv 0.23 1
rs11644758
LOC105371356
16 79675094 upstream gene variant A/C snv 0.34 1
rs12471433
MIR3128 ; NFE2L2
2 177257637 intron variant A/C snv 0.29 1
rs12920176
LOC105371257
16 51727173 intergenic variant A/C snv 0.33 1
rs150457564
HOXD1 ; MIR7704 ; HAGLR
2 176188698 5 prime UTR variant A/C snv 2.5E-02 2.2E-02 1
rs1541937
OR52B5P
11 5557328 intron variant A/C snv 0.36 1
rs199796575
MRTFA ; COX6B1P3
22 40569767 intron variant A/C snv 7.5E-02 1