Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10062079
C9 ; DAB2
5 39393631 intron variant G/A snv 0.39 1
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs10127790
SORT1
1 109348511 intron variant C/T snv 0.63 2
rs10206899
ALMS1P1
2 73673773 intron variant T/C;G snv 0.21; 3.9E-05 3
rs10254101
PRKAG2
7 151718450 intron variant C/T snv 0.23 3
rs10262995
BBS9
7 33510429 intron variant C/T snv 9.1E-02 1
rs10277115 7 1245559 regulatory region variant A/T snv 0.57 2
rs1044261
GTPBP4 ; IDI2
1.000 0.080 10 1019770 stop gained C/T snv 5.0E-02 6.0E-02 3
rs10459012 11 55324098 upstream gene variant C/A snv 0.25 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs10491967
TSPAN9
12 3258927 intron variant G/A snv 0.21 2
rs10513801
ETV5
3 186104564 intron variant T/G snv 9.2E-02 3
rs10518732
WDR72
15 53646845 intron variant G/A;C snv 2
rs10518733
WDR72
15 53648110 intron variant A/C;G snv 1
rs10746942
PIP5K1B
9 68819549 intron variant G/A snv 0.63 2
rs10774021
SLC6A13
1.000 0.080 12 240132 intron variant C/T snv 0.57 4
rs10794486
IGF1R
15 98758306 intron variant G/A;T snv 1
rs10794720
WDR37
1.000 0.080 10 1110225 intron variant T/C snv 0.89 4
rs10840341 11 2095263 intergenic variant T/A;C snv 2
rs10851885
NRG4
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18 5
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs10874312 1 82478888 intron variant G/A snv 0.70 3
rs10994856
A1CF
0.925 0.120 10 50885488 intron variant G/A snv 0.19 5
rs10994860
A1CF
0.925 0.120 10 50885664 5 prime UTR variant C/T snv 0.19 5
rs11062167
LOC102723544 ; SLC6A13
12 255573 intron variant G/A snv 0.36 2