Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs754320812
FBXL6 ; SLC52A2
0.925 8 144360427 missense variant T/C snv 2.4E-05 3.5E-05 4
rs758432471
GNB1
0.925 1 1806513 missense variant C/T snv 7.0E-06 4
rs777218310
ECHS1
0.925 10 133369907 frameshift variant TA/- delins 1.6E-05 1.3E-04 4
rs786205208
NEXMIF
0.925 X 74742675 stop gained G/A snv 4
rs797044854
ZMYND11
0.925 10 252459 missense variant C/A;T snv 4
rs797044884
PTRH2 ; CLTC
0.925 17 59677123 frameshift variant -/GA delins 4
rs797044885
ZBTB18
0.925 1 244055156 missense variant A/G snv 4
rs864321692
WAC
0.925 10 28583498 stop gained C/A snv 4
rs886041081
SLC25A4
0.925 4 185144891 missense variant G/A snv 4
rs886041877
PTEN
1.000 10 87894025 missense variant A/C;G snv 4
rs1064795935
COL4A1
1.000 13 110181389 missense variant C/T snv 3
rs1131690805
H1-4 ; H2BC5
0.925 6 26156815 frameshift variant -/G delins 3
rs115079861
RMND1
1.000 6 151405236 stop lost C/G;T snv 2.0E-05; 4.0E-03 3
rs1156904586
ATP8A2
1.000 13 25577115 frameshift variant -/T delins 1.4E-05 3
rs1158141270
NALCN
0.925 13 101061967 splice donor variant C/A snv 4.0E-06 3
rs1182326570
FBXL4
0.925 6 98926883 stop gained T/A snv 8.0E-06 3
rs1242562412
ERBB2 ; PGAP3
1.000 17 39687906 stop gained C/A snv 2.1E-05 3
rs1304422857
UBE3B
1.000 12 109511304 splice donor variant G/A;T snv 3
rs1313319892
POGZ
1.000 1 151406306 stop gained G/A;T snv 7.0E-06 3
rs1350201776
ZNF335
20 45952244 missense variant C/T snv 4.0E-06 3
rs1382415023
SON
1.000 21 33554945 frameshift variant GAAA/- delins 3
rs142684762
ADGRG1
1.000 16 57659478 missense variant A/G snv 3
rs1462161137
METTL23
1.000 17 76733042 frameshift variant -/A delins 7.0E-06 3
rs1468358104
FLVCR1 ; FLVCR1-DT
1 212858454 start lost T/C snv 3.7E-05 3
rs147334255
MN1
1.000 22 27750995 stop gained G/A snv 3