Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 19
rs9330813
WNT7B
1.000 0.040 22 45968281 intron variant G/A;C snv 4
rs1536482 1.000 0.040 9 134548682 upstream gene variant G/A snv 0.36 3
rs4608502
COL4A3 ; MFF-DT
2 227269439 intron variant T/A;C snv 3
rs12447690
LOC107984862
1.000 0.160 16 88264518 intron variant C/T snv 0.53 3
rs10453441
WNT7B
1.000 0.040 22 45967859 intron variant A/G snv 0.40 3
rs12448211 16 88296907 intron variant G/A snv 0.56 2
rs28687756 16 88295322 intron variant T/G snv 6.5E-04 2
rs3118520 9 134549749 upstream gene variant A/G snv 0.49 2
rs4792535 17 14661813 intergenic variant C/T snv 0.45 2
rs4938174 11 111042516 upstream gene variant G/A snv 0.31 2
rs7040970 9 136964561 upstream gene variant T/C snv 0.44 2
rs56009602
ADAMTS8
11 130419717 intron variant C/A;T snv 2
rs752092
CHSY1
15 101241729 intron variant A/G snv 0.43 2
rs96067
COL8A2
1 36106319 intron variant G/A snv 0.73 2
rs11553764
GLT8D2
12 104021466 5 prime UTR variant C/T snv 0.13 2
rs9822953
LINC00886
3 156754282 intron variant C/G;T snv 2
rs3118515
LOC100506532
9 134544468 intron variant G/A;C;T snv 2
rs4841899
LOC100506532
9 134532566 intron variant T/C snv 0.32 2
rs930847
LRRK1
15 101018357 intron variant G/T snv 0.67 2
rs785422
TJP1
15 29881682 intron variant C/T snv 1.0E-01 2
rs10161679 13 22669506 intergenic variant G/A;C snv 1
rs13024279 2 234563951 intergenic variant A/G snv 0.47 1
rs16920206 10 64725315 intergenic variant T/C snv 2.3E-02 1
rs2106166 7 93039018 intergenic variant A/T snv 0.44 1