Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28939688
OPTN
0.807 0.040 10 13109270 missense variant G/A snv 7
rs4656461 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 7
rs199746824
MYOC
0.807 0.040 1 171652139 missense variant C/G;T snv 4.0E-06; 1.6E-05 6
rs11656696
GAS7
0.882 0.040 17 10130362 intron variant C/A snv 0.36 5
rs16947
NDUFA6-DT ; CYP2D6
0.882 0.040 22 42127941 missense variant G/A;T snv 5
rs1900004
LINC02640
0.827 0.040 10 68241124 intron variant C/T snv 0.39 5
rs2472493
LOC105376196
0.851 0.040 9 104933567 downstream gene variant G/A snv 0.61 5
rs10483727 0.851 0.040 14 60606157 upstream gene variant T/C snv 0.45 4
rs1192415 0.925 0.040 1 91611540 TF binding site variant G/A snv 0.81 4
rs2234927
MYOCOS ; MYOC
0.851 0.040 1 171638703 missense variant G/A;C snv 4.0E-06; 7.6E-04 4
rs3793342
NOS3
0.851 0.040 7 150998107 intron variant G/A snv 0.13 4
rs4236601 0.882 0.040 7 116522675 upstream gene variant G/A snv 0.28 4
rs6445055
FNDC3B
0.925 0.040 3 172274597 intron variant G/A snv 0.24 4
rs7081455 0.851 0.040 10 20349956 upstream gene variant G/A;T snv 4
rs74315334
MYOCOS ; MYOC
0.851 0.040 1 171636341 missense variant C/T snv 4
rs74315336
MYOCOS ; MYOC
0.851 0.040 1 171636173 missense variant T/C snv 4
rs74315341
MYOC ; MYOCOS
0.851 0.040 1 171636686 missense variant C/T snv 4
rs747782 0.925 0.040 11 47919373 intergenic variant T/C snv 0.26 4
rs75654767
OPTN
0.851 0.040 10 13136766 missense variant G/A snv 3.1E-03 1.0E-03 4
rs10038177
WDR36
0.925 0.040 5 111100751 intron variant C/T snv 0.53 0.54 3
rs1052990
CAV2
0.882 0.040 7 116508316 3 prime UTR variant T/C;G snv 3
rs11241095
WDR36
0.925 0.040 5 111103810 missense variant A/C;G snv 0.33 3
rs11568658
SNORD13G ; ABCC4
0.925 0.040 13 95210754 missense variant C/A snv 4.9E-02 3.0E-02 3
rs11669977
NTF4
0.882 0.040 19 49060867 non coding transcript exon variant A/G snv 0.17 3
rs11720822
PDIA5
0.882 0.040 3 123150194 intron variant C/T snv 8.6E-02 6.6E-02 3