Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
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
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5
rs66505542
BUD13
11 116752498 intron variant AA/-;A;AAA delins 5
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 4
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 4
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 4