Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 7
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6