Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228292
CLCN2
1.000 3 184352800 missense variant C/G snv 1.5E-02 1.6E-02 1
rs3735273
DDC ; FIGNL1
1.000 7 50529166 intron variant C/T snv 0.25 0.27 1
rs1248634
DLG5
1.000 10 77819464 splice region variant G/A snv 0.29 0.24 1
rs773941026
FGF14
1.000 13 102401633 missense variant A/G;T snv 2.4E-05 1
rs1213743797
GLI3
1.000 7 41964929 missense variant C/G snv 4.0E-06 1
rs982730623
GPD1L
1.000 3 32146681 stop gained C/T snv 1
rs753721001
HSF2
1.000 6 122399830 missense variant G/A;C snv 4.1E-06; 4.1E-06 1
rs1159077388
MPHOSPH6
1.000 16 82164193 missense variant A/T snv 4.3E-06 1
rs1057519980
TP53
1.000 17 7675084 missense variant G/C snv 1
rs770029606
VPS35
1.000 16 46674629 missense variant G/A snv 7.7E-05 9.2E-05 1
rs757196717
ADRA1A
0.925 0.040 8 26770273 missense variant C/G;T snv 4.0E-06 2
rs767958027
ADRA2B
0.925 0.040 2 96114892 missense variant A/T snv 2
rs587777741
ANLN
0.925 7 36411062 missense variant C/T snv 1.7E-05 3.5E-05 2
rs200074159
APP
0.925 0.080 21 26000036 missense variant T/C snv 2.8E-05 5.6E-05 2
rs782175860
ATP1A3
0.925 19 41975776 missense variant C/T snv 2
rs778581081
ATP2A3
0.925 17 3937577 missense variant C/T snv 4.0E-06 2
rs1202752581
BECN1
0.925 0.040 17 42820818 missense variant C/T snv 7.0E-06 2
rs80357033
BRCA1
0.925 0.200 17 43106467 missense variant A/C;G snv 2
rs964793521
CASP3
0.925 0.080 4 184638460 5 prime UTR variant C/T snv 1.4E-05 2
rs4434401
CAST
0.925 0.040 5 96703321 intron variant T/C snv 0.45 2
rs1345128632
CNP
0.925 0.080 17 41968217 synonymous variant G/A snv 7.0E-06 2
rs758847245
COQ2
0.925 0.040 4 83267696 missense variant C/T snv 6.1E-06 4.9E-05 2
rs766552045
COQ2
0.925 0.040 4 83284854 missense variant C/T snv 5.3E-05 2.1E-05 2
rs3837091
DDC
1.000 7 50561043 5 prime UTR variant TCTC/-;TC delins 0.23 2
rs200945454
EDNRA
0.925 0.040 4 147542593 missense variant G/A;C snv 2