Source: ALL
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-02 262
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 15
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34 7
rs2763981
CYP21A2 ; SLC44A4
6 31872244 intron variant T/A snv 0.79 5
rs116009877 6 25715429 regulatory region variant G/A;T snv 4
rs71559014 6 27154665 regulatory region variant A/G snv 4.2E-02 4
rs13191659
LINC00240
6 27033276 intron variant C/G;T snv 4
rs6762719
TF
3 133761973 non coding transcript exon variant A/G snv 0.31 4
rs80215559
SLC17A2
6 25917997 intron variant T/C snv 3.7E-02 3
rs8177248
TF
1.000 0.040 3 133760782 non coding transcript exon variant C/T snv 0.28 3
rs8177253
TF
1.000 0.040 3 133761348 non coding transcript exon variant C/T snv 0.31 3
rs12052498 2 189497185 intergenic variant G/A snv 0.39 2
rs144403535 2 62178025 regulatory region variant A/G snv 3.8E-03 2
rs2698530 2 64276761 intergenic variant A/C snv 0.23 2
rs61784830 1 45763401 intergenic variant G/A snv 8.9E-02 2
rs78455250 1 189052039 intergenic variant G/A;C snv 2
rs183360145
CARMIL1 ; CMAHP
6 25296893 intron variant T/C snv 2.6E-03 2
rs56071727
CCDC17
1 45625172 upstream gene variant G/T snv 9.0E-02 2
rs187281066
CPNE4
3 132157410 intron variant A/G snv 1.4E-05 2
rs112409831
DNAJC13
3 132417596 5 prime UTR variant C/T snv 2.3E-02 2
rs183252871
EPHB1
3 134964503 intron variant T/C;G snv 2
rs187472012
EPHB1
3 134820915 intron variant A/G snv 2.7E-04 2
rs78545713
H4C7
6 26248612 upstream gene variant A/G;T snv 2
rs9813476
LMLN
3 197992314 intron variant C/T snv 3.7E-02 2