Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs35789010
CARMIL1
0.851 0.200 6 25513951 intron variant G/A snv 4.1E-02 7
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 6
rs2032447
H3C3 ; H2BC3 ; H2AC5P
0.925 0.120 6 26044141 non coding transcript exon variant A/G snv 4.1E-06; 0.67 0.67 6
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 6
rs1541374 4 105127203 intergenic variant T/A;G snv 5
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 5
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs7359397
SH2B1
1.000 0.040 16 28874338 upstream gene variant C/T snv 0.28 5
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 4
rs6012558 20 48914749 intergenic variant G/A snv 0.42 4
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4