Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs116009877 6 25715429 regulatory region variant G/A;T snv 4
rs13191659
LINC00240
6 27033276 intron variant C/G;T snv 4
rs138584487
LARGE1
22 33416876 intron variant G/A;C snv 1
rs3013795
ANTXRL
10 46313639 intron variant T/A;G snv 1
rs4642515
HLA-DQB1
6 32664039 non coding transcript exon variant T/A;G snv 1
rs181143083
ZDHHC14
6 157434218 intron variant T/A snv 7.5E-04 2
rs3797579
POLK
5 75574232 intron variant A/G snv 9.9E-04 1
rs147477420 11 33988237 TF binding site variant G/A snv 3.2E-03 1
rs144453006
SLC3A2
11 62887212 intron variant G/A snv 3.2E-03 1
rs116112266
LINC01885
2 107482651 intron variant G/C snv 3.5E-03 1
rs184908836
LINC02008
3 82041833 intron variant A/G snv 3.8E-03 1
rs150548770
ESM1 ; LOC102467081
5 55020802 intron variant T/C snv 5.4E-03 2
rs143130997
FIG4
6 109780207 intron variant G/A snv 5.9E-03 2
rs140911738
MAPRE1
20 32849813 3 prime UTR variant G/C snv 9.3E-03 1
rs10097946
KCNU1 ; LOC105379375
8 36920273 intron variant C/A snv 1.0E-02 1
rs111991936 7 23289983 regulatory region variant G/A snv 1.1E-02 1
rs10101752 8 37125160 intergenic variant G/A snv 1.2E-02 1
rs73214671
SORCS2
4 7570384 intron variant G/A snv 1.5E-02 1
rs202056061
CARMIL1
6 25494109 intron variant AGTT/- delins 2.8E-02 2
rs73373322
SEPTIN9
17 77385957 intron variant C/T snv 3.1E-02 2
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 15
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs17052130
SPRY3
X 155675419 intergenic variant T/C snv 4.0E-02 1
rs141555380
GAB3
X 154677735 3 prime UTR variant C/T snv 4.2E-02 1