Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25 4
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 4
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42 4
rs7132908
FAIM2
1.000 0.080 12 49869365 3 prime UTR variant G/A snv 0.31 4
rs1573891 15 98643259 downstream gene variant G/C snv 0.32 3
rs34776209 7 23473474 upstream gene variant C/T snv 0.18 3
rs9525638 13 42554441 regulatory region variant T/C snv 0.37 3
rs16942341
ACAN
15 88845674 synonymous variant C/T snv 3.8E-02 6.4E-02 3
rs6570509
ADGRG6
6 142395149 intron variant G/T snv 0.41 3
rs12513481
AP3B1
5 78155004 intron variant G/C snv 0.19 3
rs11030119
BDNF
11 27706555 intron variant G/A;T snv 3
rs3814333
COLGALT2
1 184037985 upstream gene variant C/T snv 0.29 3
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 3
rs3818416
EDNRB-AS1 ; EDNRB
1.000 0.080 13 77900333 intron variant A/C snv 0.75 3
rs917727
FAM3C
7 121378525 intron variant C/A;T snv 0.33 3
rs7996639
HS6ST3
13 96366836 intron variant G/A snv 0.50 3
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs35506085
IGF2 ; INS-IGF2 ; IGF2-AS
11 2144346 intron variant G/A snv 0.17 3
rs7952436
KDM2A
11 67257063 3 prime UTR variant C/T snv 4.7E-02 3
rs1056513
PATJ
1 61914626 missense variant G/A;C snv 0.57; 8.0E-06 3
rs72656010
PLAG1 ; CHCHD7
8 56209656 intron variant T/C snv 0.10 3
rs11187838
PLCE1-AS1 ; PLCE1
10 94278929 non coding transcript exon variant G/A snv 0.44 3
rs5750823
TAB1 ; LOC100506472
22 39433968 intron variant C/T snv 0.70 3
rs147110934
ZNF628
19 55482069 missense variant G/T snv 1.4E-02 1.5E-02 3
rs12741884 1 22268202 downstream gene variant G/A;C snv 2