Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs523349
SRD5A2
0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs11558538
LOC107985948 ; HNMT
0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs9282858
SRD5A2
0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 16
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs11681792
NRXN1
1.000 0.080 2 49957256 intron variant C/T snv 0.12 4
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4
rs371308207
C1D
0.882 0.080 2 68047303 missense variant C/A;T snv 4.1E-06; 4.1E-06 4
rs55702914 0.925 0.080 2 197349672 intergenic variant C/G snv 0.37 4
rs10211296
CSRNP3
1.000 0.080 2 165633833 intron variant A/G snv 0.34 3
rs1437396 1.000 0.080 2 55278320 upstream gene variant C/G;T snv 3
rs1660895 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 3
rs181048070
LOC105374754
1.000 0.080 2 59316241 intron variant G/A snv 1.4E-02 3
rs2253612
AOX3P ; AOX3P-AOX2P
1.000 0.080 2 200703710 intron variant C/T snv 0.79 3
rs35349697
CREB1
0.882 0.080 2 207560294 synonymous variant G/A snv 8.0E-06 3
rs3771856
TACR1 ; LOC105374811 ; LOC105374812
0.882 0.080 2 75186888 non coding transcript exon variant G/A snv 0.57 3
rs540606 1.000 0.080 2 44911368 intergenic variant A/G snv 0.66 3
rs570436 1.000 0.080 2 44915534 intergenic variant C/T snv 0.69 3
rs6716455
LINC01818
1.000 0.080 2 150269889 intron variant G/A snv 0.11 3
rs7590720
PECR ; MREG
1.000 0.080 2 216033935 intron variant G/A snv 0.73 3
rs896543
LOC107986001
1.000 0.080 2 236600564 intergenic variant G/A snv 0.33 3
rs3917328
IL1R1
1.000 0.080 2 102178081 3 prime UTR variant C/G;T snv 5.1E-02 2
rs56013859
PER2
0.925 0.080 2 238276865 intron variant T/C snv 0.11 2