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
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 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
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs13412535
SERPINE2
2 224010157 intron variant G/A snv 0.17 5
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 5
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs56043070
GCSAML
1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 4