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
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
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
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
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
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5