Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 10
rs11789015
BARX1
0.882 0.080 9 93953746 intron variant A/C;G snv 6
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv 6
rs10419226
CRTC1
0.925 0.080 19 18692362 intron variant T/G snv 0.67 5
rs11901649
APOB
0.882 0.080 2 21027351 intron variant G/A;C;T snv 3
rs17451754
CFTR
0.925 0.080 7 117616658 intron variant G/A snv 0.10 2
rs17749155
MSRA
0.925 0.080 8 10210563 intron variant G/A snv 0.16 2
rs199620551
CRTC1
0.925 0.080 19 18693485 intron variant G/- del 9.2E-02 2
rs2464469
LOC283665 ; ALDH1A2
0.925 0.080 15 58069827 intron variant G/A snv 0.65 2
rs2518720
CDKN2A
0.925 0.080 9 21978980 intron variant C/T snv 0.43 2
rs7852462
TMOD1
0.925 0.080 9 97548219 intron variant C/A;T snv 2
rs11631094
SLC12A6
1.000 0.080 15 34332237 intron variant G/C;T snv 1
rs1548445
VPS35L
1.000 0.080 16 19680261 intron variant A/G snv 0.17 1
rs66725070
ALDH1A2
1.000 0.080 15 57975219 intron variant ACAT/- delins 0.35 1
rs717746
CDX1
1.000 0.080 5 150176995 intron variant T/A;C;G snv 1
rs9668109
IKBIP
1.000 0.080 12 98617494 intron variant G/A snv 0.15 1
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 6
rs9936833 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 6
rs4800353 0.925 0.080 18 22074176 intergenic variant A/G snv 0.30 5
rs4676893 0.882 0.080 3 70868488 intergenic variant A/T snv 0.61 3
rs62423175 0.925 0.080 6 61485463 intergenic variant G/A snv 2
rs6449586 1.000 0.080 5 51339044 intergenic variant C/T snv 0.64 1
rs2687202 0.925 0.080 3 70880832 regulatory region variant T/C snv 0.64 2
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262