Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28584580
ACAN
15 88854596 intron variant A/G snv 0.11 2
rs3027009
ACKR1 ; CADM3-AS1
1 159204097 intron variant A/G snv 5.8E-02 2
rs62621197
ADAMTS10
1.000 0.080 19 8605262 missense variant C/A;T snv 4.1E-06; 3.1E-02 2.9E-02 4
rs34821335
ADAMTS14
10 70673448 intron variant A/- del 0.20 1
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs4988781
ADAMTS17
15 100260635 intron variant A/C snv 0.68 1
rs888762
ADAMTS2
5 179120312 3 prime UTR variant C/A;G;T snv 1
rs11856122
ADAMTSL3
15 83907596 intron variant G/A snv 0.63 1
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs10584116
AFG3L1P
16 89995916 non coding transcript exon variant CT/- delins 0.14 1
rs798491
AMZ1 ; GNA12
7 2760887 intron variant A/C;G snv 2
rs34341
ANKDD1B
5 75638184 intron variant A/T snv 0.43 1
rs34716573
B4GALNT3
12 466871 intron variant T/C snv 0.32 1
rs10962638
BNC2
9 16846113 intron variant G/A;C snv 1
rs12794995
C11orf72 ; NDUFV1
11 67605475 intron variant G/A;T snv 1
rs465983
C5orf67
5 56516303 intron variant A/G snv 0.27 2
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 4
rs6085551
CASC20
20 6428273 intergenic variant T/C snv 0.48 1
rs11049566
CCDC91
12 28380028 intron variant C/T snv 0.19 1
rs527582137
CDK6
7 92622008 intron variant TT/-;T;TTT;TTTT;TTTTTTTTT delins 1
rs10402308
CILP2
19 19546691 downstream gene variant G/A snv 0.27 1
rs1138714
CRACR2B ; PNPLA2
11 825110 3 prime UTR variant A/G snv 0.47 1
rs543860487
CREB3L2
7 137904839 intron variant AAA/-;A;AA;AAAA;AAAAA;AAAAAA delins 1
rs545608
CRYZL2P-SEC16B ; SEC16B
0.925 0.040 1 177929986 intron variant G/C snv 0.20 4
rs754537
DNAJC27
2 24953408 intron variant A/T snv 0.41 1