Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8054556
TMEM219
0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs9844972 1.000 0.080 3 150379848 regulatory region variant G/A;C snv 4
rs10980797
LOC105376219
9 111150273 intron variant A/G;T snv 3
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 3
rs12608504 19 18278325 upstream gene variant A/G;T snv 3
rs2928140
RAD51
0.925 0.080 15 40698155 intron variant G/C;T snv 3
rs3936510
C5orf67
1.000 0.040 5 56565039 intron variant G/A;T snv 3
rs984222
TBX15
1 118961220 intron variant C/A;G snv 3
rs10152595
SMAD3
1.000 0.080 15 67183150 intron variant C/G;T snv 2
rs1044299
PAPPA2
1 176842737 3 prime UTR variant C/G;T snv 2
rs1053593
HMGXB4
22 35264882 missense variant G/C;T snv 8.0E-06; 0.58 2
rs10876528
HOXC6 ; HOXC5 ; HOXC4
12 54027692 intron variant C/A;G snv 2
rs11085744
QTRT1
19 10709291 missense variant C/G;T snv 0.53 2
rs12042959
SDCCAG8
1 243369971 intron variant A/G;T snv 2
rs12214804 6 34221089 downstream gene variant C/A;G;T snv 2
rs12440667
LOXL1
1.000 0.040 15 73939098 intron variant C/A;T snv 2
rs12495178
CADM2
3 85836927 intron variant T/A;C snv 2
rs1278493
PPP2R3A
1.000 0.080 3 136095167 intron variant G/A;C snv 2
rs12868881 13 111566577 intergenic variant T/A;C snv 2
rs1294421
LOC101928004
1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 2
rs1345203
SOCAR ; MIR4435-2HG
2 111496274 intron variant T/C;G snv 2
rs17264866
PPIEL
1 39557105 intron variant C/A;G snv 2
rs17448885
KLHL32
6 96938099 intron variant C/A;G snv 2
rs17568628 5 76751114 intergenic variant T/C;G snv 2