Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4792795
TBC1D27P
17 16922702 downstream gene variant A/G snv 0.16 2
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 2
rs7786877 7 100616392 downstream gene variant A/G snv 0.22 2
rs9310736
THRB
3 24309320 intron variant A/G snv 0.69 2
rs9389268
HBS1L
1.000 0.080 6 135098493 intron variant A/G snv 0.24 2
rs10207392
ACOXL ; MIR4435-2HG
2 111092082 intron variant A/G snv 0.48 1
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 1
rs16895130
CCND3
6 41957193 intron variant A/G snv 0.22 1
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 1
rs346522 19 43758393 upstream gene variant A/G snv 0.33 1
rs3827335
FBXO7
22 32487295 non coding transcript exon variant A/G snv 0.55 1
rs732716
SH3GL1
19 4366222 intron variant A/G snv 0.23 1
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 5
rs9483769
LOC101928277
6 134878643 intergenic variant A/G;T snv 3
rs9349204
CCND3
6 41946640 intron variant A/G;T snv 2
rs218238 4 54528857 intergenic variant A/T snv 0.38 2
rs7189020
FAM234A
16 254804 intron variant A/T snv 0.55 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 6
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 5
rs628751 6 139517282 intron variant C/A snv 0.41 2
rs381500
LOC105378102
6 164057356 intergenic variant C/A snv 0.46 1