Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs461155
ETS2
0.925 0.120 21 38819714 synonymous variant A/G;T snv 0.72; 4.0E-06 3
rs6962966
MAGI2
0.925 0.120 7 78174806 intron variant A/G snv 0.50 3
rs10763976
PARD3
0.925 0.120 10 34275364 intron variant G/A snv 0.42 2
rs11254
ETS2
0.925 0.120 21 38824464 3 prime UTR variant C/T snv 0.34 2
rs1215380342
SLC19A1
0.925 0.120 21 45531505 missense variant G/A snv 8.0E-06 2
rs1331959399
TWIST1
0.925 0.120 7 19117256 synonymous variant T/C snv 2
rs1445106099
SLC19A1
0.925 0.120 21 45531596 missense variant C/T snv 4.0E-06 2
rs1496770
MAGI2
0.925 0.120 7 78629694 intron variant C/T snv 0.43 2
rs199683090
SLC19A1
0.925 0.120 21 45531476 missense variant C/T snv 2
rs2070531
ETS2
0.925 0.120 21 38822292 intron variant C/T snv 0.35 2
rs2073416
SIM2
0.925 0.120 21 36744739 synonymous variant G/A;T snv 0.22 2
rs2073601
SIM2
0.925 0.120 21 36745007 missense variant C/A;T snv 0.28; 2.4E-05 2
rs778423815
TP73
0.925 0.120 1 3707661 missense variant C/G snv 4.4E-05 1.4E-05 2
rs9640699
MAGI2
0.925 0.120 7 78366115 intron variant A/C snv 0.58 2
rs121912594
CPS1
0.882 0.160 2 210675762 missense variant A/C snv 7
rs104893904
NKX2-5
0.807 0.160 5 173235023 missense variant C/G snv 1.1E-03 7.1E-04 6
rs373667881
TRIB1
0.827 0.160 8 125431222 missense variant G/A;T snv 1.1E-03 5
rs1323833193
EGF
0.851 0.160 4 109994859 missense variant C/G snv 4.0E-06 4
rs3774207
CRELD1
0.851 0.160 3 9943972 synonymous variant C/T snv 0.27 0.38 4
rs73118372
CRELD1
0.851 0.160 3 9943989 missense variant T/C;G snv 2.6E-02; 6.8E-05 4
rs755981922
CRELD1
0.851 0.160 3 9943440 missense variant G/A snv 8.0E-06 2.1E-05 4
rs9878047
CRELD1
0.851 0.160 3 9943773 intron variant T/C snv 0.38 4
rs142569954
EDNRB
0.882 0.160 13 77918396 missense variant C/G;T snv 4.1E-06; 2.1E-05 3
rs2506004
RET
0.882 0.160 10 43086825 intron variant A/C;T snv 3
rs363430
BACH1 ; GRIK1-AS2 ; GRIK1
0.882 0.160 21 29598863 synonymous variant G/A snv 0.18 0.17 3