Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2414095
CYP19A1 ; MIR4713HG
15 51232095 intron variant A/G snv 0.69 4
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs6959212 7 38088724 intergenic variant T/C;G snv 4
rs72699866
RIN3
14 92648442 intron variant G/A snv 0.14 4
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 4
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv 3
rs12283755
PPP6R3
11 68604190 intron variant A/G snv 0.24 3
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 3
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 3
rs1564981 16 50952397 intergenic variant G/A snv 0.60 3
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv 3
rs4580892 6 127088737 intron variant C/T snv 0.32 3
rs4720530
WIPI2
7 5212643 intron variant C/T snv 0.55 3
rs6894139
MEF2C-AS1
5 89031965 non coding transcript exon variant T/G snv 0.57 3
rs7466269
FUBP3
9 130588697 intron variant A/G snv 0.33 3
rs917727
FAM3C
7 121378525 intron variant C/A;T snv 0.33 3
rs9525638 13 42554441 regulatory region variant T/C snv 0.37 3
rs9533090
LINC02341
13 42377313 intron variant C/T snv 0.39 3
rs10048745
ARHGAP25
2 68735005 5 prime UTR variant G/A snv 0.24 2
rs1021188 13 42541997 intergenic variant C/T snv 0.79 2
rs10226308
EPDR1 ; NME8
7 37898820 intron variant A/C;G snv 2
rs10242100 7 121343289 downstream gene variant A/G snv 0.29 2
rs10416218
GPATCH1
19 33108221 intron variant T/C snv 0.42 2
rs10429035
SEM1 ; LOC105375411
7 96490169 intron variant G/A snv 0.39 2
rs10502386 18 8966146 intergenic variant G/T snv 0.39 2