Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs142322800
FCGR3A
1 161548502 missense variant T/C snv 1.5E-04 5.6E-05 1
rs757956956
GPI
19 34377533 missense variant A/G snv 4.0E-06 1
rs12329305
OSR1
2 19353152 synonymous variant C/A;T snv 1.6E-04; 5.5E-02 1
rs504849
WNT5A
3 55488911 intron variant T/C;G snv 1
rs524153
WNT5A
3 55491957 upstream gene variant T/A;G snv 1
rs1234344050
COL3A1 ; LOC105373791
2 188984825 missense variant C/G snv 4.0E-06 2
rs387906617
CREB1
2 207567506 missense variant A/G snv 2
rs764120087
EP300
22 41117439 missense variant G/A snv 8.0E-06 2
rs137854438
FAM83H
1.000 0.080 8 143728570 stop gained A/T snv 2
rs1206736425
FCGR3B
1 161626229 missense variant T/C snv 2
rs1387329667
NOTCH1
9 136500595 missense variant G/A snv 2
rs756434709
NOTCH1
9 136514670 missense variant C/T snv 2.0E-05 7.0E-06 2
rs769269532
SOX9-AS1 ; SOX9
1.000 0.040 17 72124262 missense variant A/G snv 2.4E-05 1.4E-05 2
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
rs201968272
DDX11
0.925 0.160 12 31089147 missense variant G/A snv 3
rs201405525
DECR1
0.925 0.240 8 90044993 missense variant G/A;C snv 4.5E-04; 4.0E-06 3
rs121918214
FTO
1.000 0.200 16 53873837 missense variant G/A snv 4.0E-06 7.0E-06 3
rs745616565
FTO
1.000 0.200 16 53873855 missense variant G/A snv 1.6E-05 2.1E-05 3
rs781028867
FTO
1.000 0.200 16 53873846 missense variant C/A;T snv 4.0E-06 3
rs121909497
MMP13
0.925 0.080 11 102955390 missense variant A/G snv 3
rs1057517786
PDCD10
0.925 0.400 3 167704889 stop gained G/A snv 3
rs587777186
PIGN
0.925 18 62146023 missense variant A/G;T snv 3
rs774753616
PIGT ; LOC107985405
1.000 20 45419351 missense variant G/A snv 1.2E-05 1.4E-05 3
rs869025322
PIGY ; PYURF
0.925 0.040 4 88521653 missense variant A/G snv 3