Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 8
rs8037137
RCCD1
0.807 0.160 15 90963407 upstream gene variant T/C snv 0.19 8
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs342293
CTB-30L5.1
0.882 0.040 7 106731773 intron variant C/G snv 0.42 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
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 6
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42 6
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 5
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs66505542
BUD13
11 116752498 intron variant AA/-;A;AAA delins 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 5
rs97384
FADS2
1.000 0.080 11 61856709 non coding transcript exon variant T/C snv 0.46 5
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 4
rs11405616
NDFIP1
5 142130697 intron variant A/-;AA;AAA;AAAA delins 4
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4