Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4418214 0.925 0.040 6 31423624 intron variant T/C snv 7.7E-02 4
rs10045403
ERAP1
0.882 0.040 5 96812030 upstream gene variant A/G snv 0.23 3
rs10946808
H2AC9P
1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26 2
rs35164067
CDC37
1.000 0.040 19 10414505 intron variant G/A snv 0.18 2
rs6556416 1.000 0.040 5 159391737 intron variant A/C;T snv 2
rs1013210 1.000 0.040 8 24259209 intergenic variant G/A;C;T snv 1
rs10280089 1.000 0.040 7 38667217 intergenic variant C/A;T snv 1
rs10440635 1.000 0.040 5 40490688 intron variant G/A snv 0.56 1
rs10781500
CARD9
1.000 0.040 9 136374886 upstream gene variant C/G;T snv 1
rs11065898
SH2B3
1.000 0.040 12 111424771 intron variant C/T snv 0.21 1
rs11249215 1.000 0.040 1 24970693 non coding transcript exon variant G/A snv 0.44 1
rs1128905
DNLZ ; GPSM1
1.000 0.040 9 136359387 3 prime UTR variant T/C snv 0.46 1
rs11742270 1.000 0.040 5 35881341 downstream gene variant G/A snv 0.20 1
rs117486637
HLA-B
1.000 0.040 6 31358156 upstream gene variant T/C snv 1
rs12141575 1.000 0.040 1 67281753 downstream gene variant G/A snv 0.31 1
rs12504282
ANTXR2
1.000 0.040 4 80005847 intron variant C/G;T snv 1
rs12615545
LINC01934
1.000 0.040 2 181183725 intron variant T/A;C snv 1
rs12758027
HHAT
1.000 0.040 1 210621464 intron variant T/C snv 0.52 1
rs13001372 1.000 0.040 2 62341086 TF binding site variant A/G snv 0.59 1
rs13093489 1.000 0.040 3 27753416 intergenic variant C/A snv 0.35 1
rs13210693
CCDC162P
1.000 0.040 6 109277761 intron variant G/A snv 0.61 1
rs148783236
LOC107984741 ; USP8
1.000 0.040 15 50492819 missense variant A/C;G snv 2.5E-03 1
rs17095830
ANO6
1.000 0.040 12 45381125 intron variant A/G snv 7.9E-02 1
rs17192932
HLA-B
1.000 0.040 6 31354352 intron variant C/G snv 4.9E-02 1
rs17765610
BACH2
1.000 0.040 6 89956054 intron variant A/G snv 9.0E-02 1