Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13242458
MCM7
7 100097508 intron variant G/A snv 8.3E-02 1
rs17250196
CASTOR3 ; PVRIG ; STAG3
7 100219573 3 prime UTR variant G/A;T snv 2
rs13228694
STAG3L5P-PVRIG2P-PILRB ; STAG3L5P
7 100342684 intron variant C/G;T snv 1
rs13222543
ZCWPW1
7 100417834 intron variant C/T snv 1.2E-02 2
rs6738028
MIR4435-2HG
2 111191750 intron variant G/C snv 0.64 1
rs3981351
PLEKHS1
10 113755361 5 prime UTR variant G/A;T snv 2
rs10744816 12 114276461 regulatory region variant T/C snv 0.39 2
rs758970
MVB12B
9 126432494 intron variant A/G snv 0.58 2
rs1624802 12 130012927 intergenic variant A/G;T snv 2
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs7860634
LHX3
9 136197833 intron variant G/A snv 0.55 4
rs9497965
SASH1
1.000 0.040 6 148200156 regulatory region variant C/T snv 0.40 3
rs10032216
LOC107986195
4 148748354 intron variant T/A;C snv 3
rs12659622
FBXL7
5 15618072 intron variant G/A snv 8.3E-02 2
rs753760
PDE10A
6 165632995 intron variant C/A;G snv 2
rs11726248 4 170132368 intergenic variant G/A snv 6.8E-02 3
rs10799824
LOC105376819 ; LOC105376817 ; MICOS10
1 19514680 intron variant G/A snv 0.18 3
rs13015993
LOC101928278
2 216760800 intron variant G/A snv 0.64 2
rs7608623
ATAD2B
2 23726083 intergenic variant G/T snv 0.57 2
rs11031002
LOC105376607
11 30193714 intron variant T/A snv 0.10 2
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs12294104
LOC102723403
11 30361352 intergenic variant C/T snv 0.14 4
rs7825175
NRG1
8 32558756 intron variant G/A snv 0.18 2
rs1537424
LINC00609
1.000 0.040 14 36104812 intron variant C/T snv 0.49 3
rs7497289
SRP14-AS1
15 40041456 intron variant G/A snv 0.21 1