Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs11200638
LOC105378525 ; HTRA1
0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs61755783
PRPH2
0.763 0.080 6 42721911 missense variant G/A snv 1.4E-05 11
rs61755792
PRPH2
0.763 0.160 6 42721821 missense variant G/A;C snv 10
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 9
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 9
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 6
rs79037040
TNFRSF10A ; LOC389641
0.807 0.160 8 23225458 non coding transcript exon variant G/A;C;T snv 6
rs943080
LOC107986598
0.807 0.040 6 43858890 TF binding site variant C/T snv 0.61 6
rs11080055
TMEM97
0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs114254831
PBX2
0.827 0.040 6 32187804 intron variant A/G snv 5
rs116503776
CYP21A2 ; SKIV2L
0.827 0.040 6 31962685 intron variant G/A snv 5
rs1626340 0.827 0.120 9 99161090 intergenic variant G/A;T snv 5
rs1800995
BEST1 ; LOC107984334
0.851 0.080 11 61955906 missense variant GC/AA mnv 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
rs72802342 0.851 0.040 16 75200974 downstream gene variant C/A snv 6.2E-02 5
rs73036519
EXOC3L2 ; MARK4
0.851 0.040 19 45245104 intron variant G/A;C snv 5
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4