Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs181705462
CYP21A2 ; STK19
0.851 0.040 6 31979250 intron variant G/C;T snv 4
rs12019136
FUT6
0.851 0.040 19 5835666 intron variant G/A snv 0.12 4
rs187328863
KCNT2
0.851 0.040 1 196411028 intron variant C/T snv 1.6E-02 4
rs8135665
LOC105373027 ; SLC16A8
0.851 0.040 22 38080269 intron variant C/T snv 0.24 4
rs140647181
LOC105374007
0.851 0.040 3 99461824 intergenic variant T/C snv 1.5E-02 4
rs6565597
NPLOC4
0.851 0.040 17 81559795 intron variant C/T snv 0.30 4
rs7803454
PILRA
0.851 0.040 7 100393925 intron variant C/T snv 0.14 4
rs2842339
RAD51B
0.851 0.040 14 68520282 intron variant G/A snv 0.90 4
rs61985136
RAD51B
0.851 0.040 14 68302482 intron variant C/T snv 0.52 4
rs5754227
SYN3
0.851 0.040 22 32709831 intron variant T/C snv 0.26 4
rs71507014
TRPM3
0.851 0.040 9 70823689 intron variant -/C;CC delins 4
rs1626340 0.827 0.120 9 99161090 intergenic variant G/A;T snv 5
rs72802342 0.851 0.040 16 75200974 downstream gene variant C/A snv 6.2E-02 5
rs61941274
ACAD10
0.827 0.160 12 111694806 intron variant G/A;T snv 5
rs62358361
C9
0.851 0.040 5 39327786 intron variant G/C;T snv 5
rs116503776
CYP21A2 ; SKIV2L
0.827 0.040 6 31962685 intron variant G/A snv 5
rs73036519
EXOC3L2 ; MARK4
0.851 0.040 19 45245104 intron variant G/A;C snv 5
rs114254831
PBX2
0.827 0.040 6 32187804 intron variant A/G snv 5
rs3138141
RDH5 ; BLOC1S1-RDH5
0.827 0.040 12 55721994 3 prime UTR variant C/A snv 0.19 0.16 5
rs11080055
TMEM97
0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs147859257
C3
0.827 0.040 19 6718135 missense variant T/G snv 2.8E-03 2.4E-03 6
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 6
rs141853578
CFI
0.807 0.040 4 109764664 missense variant C/T snv 4.2E-04 3.9E-04 6
rs943080
LOC107986598
0.807 0.040 6 43858890 TF binding site variant C/T snv 0.61 6