Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 1
rs13210247
TRAF3IP2-AS1 ; TRAF3IP2
0.882 0.280 6 111601517 non coding transcript exon variant A/G snv 0.10 1
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 1
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 5
rs13708
STX1B ; HSD3B7
1.000 0.040 16 30989488 3 prime UTR variant G/A;C snv 0.52 1
rs1473247
RNF145
1.000 0.040 5 159176563 intron variant T/C snv 0.41 1
rs151823
ERAP1
1.000 0.040 5 96824289 intron variant A/C snv 0.90 1
rs16841904
DENND1B
0.807 0.160 1 197732862 intron variant C/T snv 0.18 1
rs16861329
ST6GAL1
0.882 0.160 3 186948673 intron variant C/T snv 0.13 1
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 1
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 2
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs17716942
KCNH7
0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 1
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs181359
UBE2L3
0.882 0.080 22 21574352 intron variant G/A snv 0.21 1
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs1860545
TNFRSF1A
0.790 0.200 12 6337611 intron variant G/A snv 0.31 1