Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 8
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 8
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs2284178
HCP5
0.925 0.120 6 31464348 non coding transcript exon variant C/T snv 0.44 6
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6
rs527476195
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 6
rs7756521
DDR1
1.000 6 30880476 intron variant T/C snv 0.25 5
rs3117143
LOC100129636
0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 4
rs3749971
OR12D3 ; OR5V1
0.925 0.160 6 29374998 missense variant G/A snv 5.5E-02 5.7E-02 4
rs1233579 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 3
rs13194504 0.925 0.120 6 28662914 intergenic variant G/A snv 5.1E-02 3
rs3131093 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 3
rs6467710
DGKI
7 137519073 intron variant G/A;C snv 1
rs14158
LDLR
0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs919266
BST2
19 17403506 intron variant T/C;G snv 1