Source: INFERRED ×
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 34
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 30
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 26
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 21
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 15
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 12
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12