Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs174560
FADS1 ; FADS2
1.000 0.080 11 61814292 non coding transcript exon variant T/C snv 0.30 5
rs4587207
LINC00243
1.000 6 30799168 intron variant A/G snv 0.17 5
rs113851554
MEIS1
0.882 0.080 2 66523432 intron variant G/A;T snv 5
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02 5
rs12661667
USP49
6 41824807 intron variant C/T snv 0.20 5
rs11682175
ACTG1P22
0.925 0.040 2 57760458 intron variant T/C snv 0.38 4
rs1991556
MAPT
1.000 0.040 17 46006036 intron variant G/A snv 0.14 4
rs7939345 1.000 0.040 11 47959016 intergenic variant T/A;G snv 3
rs17817288
FTO
1.000 0.080 16 53773852 intron variant A/C;G snv 3
rs1392817
PDE4B
0.925 0.040 1 66073773 intron variant A/G snv 0.51 3
rs12963463
TCF4
1.000 0.040 18 55431862 intron variant C/G;T snv 3
rs35662245 1.000 0.040 2 146825619 intergenic variant T/A snv 0.35 2
rs7616632 3 137312395 intergenic variant T/G snv 0.41 2
rs11046205
ABCC9
12 21839392 intron variant G/A snv 0.19 2
rs75641275
DPYD
1 97861577 intron variant A/C snv 0.10 2
rs3122163
HCRTR2
6 55191570 intron variant C/T snv 0.85 2
rs17688916
LINC02210-CRHR1
17 45701314 intron variant T/A snv 0.13 2
rs62158211
LOC101927400
2 113348562 intron variant G/T snv 0.18 2
rs62158170
LOC101927400 ; LOC105373567
2 113324598 upstream gene variant A/G snv 0.18 2
rs76681500
LOC105378808
1 77247749 upstream gene variant G/A snv 0.11 2
rs3823624
MAD1L1
1.000 0.040 7 2070711 intron variant T/C snv 0.17 2
rs62061734
MAPT
1.000 0.080 17 45941122 intron variant T/A;C snv 2
rs6599077
MYRIP
3 40055127 intron variant G/A snv 0.29 2
rs694383
RGS16
1 182599069 3 prime UTR variant G/C snv 0.96 2