Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs11231693
MACROD1 ; FLRT1
11 64095140 intron variant G/A snv 0.11 4
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs12489828
NT5DC2
3 52532998 intron variant G/T snv 0.51 4
rs12885454
LOC102724934
14 29267632 non coding transcript exon variant C/A snv 0.27 4
rs1344674
ZBTB38
3 141406344 intron variant A/G snv 0.55 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs1776897 6 34227234 regulatory region variant G/T snv 0.80 4
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs2071449
HOXC4 ; HOXC5 ; MIR615
12 54034227 intron variant C/A;T snv 0.35; 4.2E-06 4
rs2294239
ZNRF3
22 29053489 intron variant A/G snv 0.36 4
rs2316205 19 40840863 non coding transcript exon variant T/C snv 0.40 4
rs2638953
CCDC91
12 28381482 intron variant G/C;T snv 4
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs3760318
ADAP2
17 30920697 intron variant G/A snv 0.39 4
rs473902
PTCH1
9 95493953 intron variant T/G snv 5.7E-02 4
rs6012558 20 48914749 intergenic variant G/A snv 0.42 4
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs7697556 4 72649596 intergenic variant T/A;C snv 4
rs8010717
LOC107984630
14 79944098 intron variant T/C snv 0.29 4
rs8066985 17 70457204 intergenic variant A/G snv 0.56 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4