Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs1993976
LINC02251
1.000 15 98063084 intron variant G/A snv 0.45 5
rs7523050
LOC107985159 ; AKNAD1 ; GPSM2
1.000 1 108875057 intron variant C/A snv 0.18 5
rs921231
SLC26A7
1.000 8 91348168 intron variant T/C snv 0.21 5
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 4
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 4
rs545608
CRYZL2P-SEC16B ; SEC16B
0.925 0.040 1 177929986 intron variant G/C snv 0.20 4
rs17511102
LOC105374465 ; CDC42EP3
2 37733470 intron variant A/G;T snv 3
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs12820906
PITPNM2
12 123008576 intron variant A/G snv 0.20 2
rs28394864
LOC102724596
1.000 0.080 17 49373413 intron variant G/A;C snv 2
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
rs35344761
PCSK5
9 75895907 intron variant C/A snv 0.10 2
rs465983
C5orf67
5 56516303 intron variant A/G snv 0.27 2
rs481806
JAZF1
7 28167681 intron variant G/T snv 0.77 2
rs4846204
KIF1B
1 10248900 intron variant C/T snv 9.3E-02 2
rs798491
AMZ1 ; GNA12
7 2760887 intron variant A/C;G snv 2
rs10916174
ZNF678
1 227616340 intron variant G/A snv 0.13 1
rs10962638
BNC2
9 16846113 intron variant G/A;C snv 1
rs11049566
CCDC91
12 28380028 intron variant C/T snv 0.19 1
rs11289753
PLCE1
10 94266428 intron variant AA/-;A;AAA delins 0.47 1
rs113640408
THBS2
6 169244314 intron variant CACACACACACA/-;CA;CACA;CACACA;CACACACA;CACACACACA;CACACACACACACA;CACACACACACACACA;CACACACACACACACACA;CACACACACACACACACACA;CACACACACACACACACACACA;CACACACACACACACACACACACA;CACACACACACACACACACACACACA;CACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACA delins 1