Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777186
PIGN
0.925 18 62146023 missense variant A/G;T snv 3
rs869025322
PIGY ; PYURF
0.925 0.040 4 88521653 missense variant A/G snv 3
rs1206736425
FCGR3B
1 161626229 missense variant T/C snv 2
rs137854438
FAM83H
1.000 0.080 8 143728570 stop gained A/T snv 2
rs1387329667
NOTCH1
9 136500595 missense variant G/A snv 2
rs387906617
CREB1
2 207567506 missense variant A/G snv 2
rs504849
WNT5A
3 55488911 intron variant T/C;G snv 1
rs524153
WNT5A
3 55491957 upstream gene variant T/A;G snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs757956956
GPI
19 34377533 missense variant A/G snv 4.0E-06 1
rs121918214
FTO
1.000 0.200 16 53873837 missense variant G/A snv 4.0E-06 7.0E-06 3
rs781028867
FTO
1.000 0.200 16 53873846 missense variant C/A;T snv 4.0E-06 3
rs201405525
DECR1
0.925 0.240 8 90044993 missense variant G/A;C snv 4.5E-04; 4.0E-06 3
rs1234344050
COL3A1 ; LOC105373791
2 188984825 missense variant C/G snv 4.0E-06 2
rs28939086
SLC26A4
0.925 0.160 7 107690220 missense variant A/C;G snv 2.0E-04; 4.0E-06 4
rs368705607
MIXL1
0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06 7
rs1052108705
TCF19 ; POU5F1
6 31165217 missense variant C/T snv 4.1E-06 2.1E-05 3
rs121918355
LTBP2
0.807 0.280 14 74555629 stop gained G/A;T snv 2.1E-05; 4.2E-06 7
rs121913483
FGFR3
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs746147592
SRPX2
1.000 0.160 X 100665627 missense variant G/A;C snv 5.5E-06 2
rs80338852
B3GLCT
0.925 0.200 13 31317599 stop gained T/A;C snv 8.0E-06 3
rs104893951
FOXC1
0.851 0.080 6 1610780 missense variant T/A;C snv 8.0E-06 5
rs764120087
EP300
22 41117439 missense variant G/A snv 8.0E-06 2
rs768746587
TCF19 ; POU5F1
6 31165136 missense variant C/T snv 8.4E-06 3
rs775144154
SLC19A1
0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38