Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5875374 6 32459228 downstream gene variant -/AC delins 0.72 2
rs34018670 16 80809337 upstream gene variant -/AG delins 0.17 2
rs75900305
LOC105370356 ; MYO16
13 109159737 intron variant -/C delins 0.25 2
rs3216780
CSF1R
5 150053837 3 prime UTR variant -/C;T ins 2
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs58904263 20 31813603 upstream gene variant -/G ins 2
rs34993178
IRF8
16 85900909 intron variant -/T delins 0.15 2
rs35761782
POC1B
12 89504600 intron variant -/T delins 0.70 2
rs7041895 1.000 0.040 9 22162795 intergenic variant A/C snv 0.47 3
rs115007843
SCD5
4 82654059 intron variant A/C snv 0.18 2
rs11686139 2 226426699 intergenic variant A/C snv 0.13 2
rs2712381
RPN1
3 128619757 downstream gene variant A/C snv 0.61 2
rs6429432
LINC02768 ; LOC105373215
1 235943941 upstream gene variant A/C snv 0.93 2
rs865483
DUSP14
17 37491071 intron variant A/C snv 0.72 2
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs2239630
CEBPE
0.925 0.160 14 23120140 upstream gene variant A/C;G snv 4
rs7288670
GGT5
22 24225858 intron variant A/C;G snv 4
rs12973608 19 18287220 upstream gene variant A/C;G snv 2
rs2062225
ACOXL
2 110993295 intron variant A/C;T snv 2
rs2228468
ACKR2 ; KRBOX1 ; CYP8B1
0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 2
rs4474742
SSH2
17 29738560 intron variant A/C;T snv 2
rs7487827
NINJ2-AS1 ; NINJ2
12 642453 intron variant A/C;T snv 2
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 8