Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs147247472
AGBL4-IT1 ; AGBL4
0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs2094081
RHBDL2
0.925 0.080 1 38927359 intron variant G/A;C snv 4
rs72737330
ESRRG
0.925 0.080 1 216600151 intron variant T/C snv 0.15 4
rs4478858
SERINC2
1.000 0.080 1 31411078 intron variant T/C snv 0.48 3
rs61776290 1.000 0.080 1 10634850 upstream gene variant C/T snv 8.7E-02 3
rs6701037 1.000 0.080 1 175150943 downstream gene variant A/C;T snv 3
rs1057302
KIAA0040
1.000 0.080 1 175157287 3 prime UTR variant A/G snv 0.38 1
rs10913569
C1orf220
1.000 0.080 1 178548873 non coding transcript exon variant A/G;T snv 1
rs11583322
STK40
1.000 0.080 1 36356711 intron variant T/C snv 0.30 1
rs17028719 1.000 0.080 1 5734948 intergenic variant A/G snv 4.8E-02 1
rs6425323 1.000 0.080 1 175155900 downstream gene variant C/T snv 0.39 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs9282858
SRD5A2
0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 7
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
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
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