Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 10
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 6
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 5
rs987710
IGLV10-54
1.000 0.040 22 22158022 intron variant G/A snv 0.61 4
rs8177240
TF
3 133758857 intron variant T/C;G snv 0.29 4
rs202056061
CARMIL1
6 25494109 intron variant AGTT/- delins 2.8E-02 2
rs111722075
CMAHP ; CARMIL1
6 25373818 intron variant C/T snv 0.11 2
rs2442120
DTWD2
5 118970884 intron variant A/C snv 0.98 2
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
rs113507773
LOC105374986
6 26255511 upstream gene variant G/A snv 0.10 2
rs7588567
NCKAP5
0.925 0.040 2 133605461 regulatory region variant T/A;C;G snv 2
rs73373322
SEPTIN9
17 77385957 intron variant C/T snv 3.1E-02 2
rs181143083
ZDHHC14
6 157434218 intron variant T/A snv 7.5E-04 2
rs146680938
DNMT3B
20 32809593 downstream gene variant C/T snv 9.4E-03 1
rs117910189
ERG
21 38606304 intron variant T/C snv 1.6E-02 1
rs142471762
HLA-DQB1
6 32663606 non coding transcript exon variant TAGGATAT/- delins 6.2E-04 1
rs210368
LOC105370504
14 53669290 intron variant C/G;T snv 1
rs41270472
NOTCH4
6 32213740 synonymous variant A/C;T snv 2.3E-02 1
rs115809796
SCGN
6 25657063 intron variant A/G snv 2.8E-02 1
rs228916
TMPRSS6
22 37109512 5 prime UTR variant C/G;T snv 1
rs2315834
ZFAT
8 134507604 intron variant C/T snv 3.3E-02 1