Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4326844
COPZ1
12 54342686 intron variant A/C;G snv 0.68 1
rs926326
CARMIL1
6 25575174 intron variant A/C;G snv 1
rs2958137
HSD17B6
12 56757545 intron variant A/C;G;T snv 2
rs11240408 1 205295408 intergenic variant A/C;G;T snv 1
rs6662263
DNM3
1 171975102 intron variant A/C;G;T snv 1
rs497453 19 56128492 upstream gene variant A/C;T snv 0.95 1
rs7811142
TSC22D4
7 100467820 synonymous variant A/C;T snv 0.16 1
rs34557412
TNFRSF13B
0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 10
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 10
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 5
rs10974808
RCL1
9 4840380 intron variant A/G snv 9.0E-02 3
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 3
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25 3
rs10220411
ACTN1-AS1
14 68985371 intron variant A/G snv 0.29 2
rs11559982
COPZ1 ; RNU6-950P
12 54317790 non coding transcript exon variant A/G snv 0.68 2
rs151361
PRELID3B ; SLMO2-ATP5E
20 59038947 intron variant A/G snv 0.24 2
rs4272720
VSTM4
10 49055156 intron variant A/G snv 0.29 2
rs4470077
LOC107984664 ; TBPL2
14 55430820 intron variant A/G snv 0.29 2