Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11024102
PLEKHA7
0.851 0.040 11 16987058 intron variant T/C snv 0.20 7
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
rs1015213 0.851 0.040 8 51974981 intron variant C/T snv 0.14 6
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
rs2472493
LOC105376196
0.851 0.040 9 104933567 downstream gene variant G/A snv 0.61 5
rs4886782
LOXL1
1.000 0.040 15 73936469 intron variant G/A snv 0.27 5
rs10483727 0.851 0.040 14 60606157 upstream gene variant T/C snv 0.45 4
rs2093210
C14orf39
1.000 0.040 14 60490561 intron variant C/T snv 0.45 4
rs2234927
MYOCOS ; MYOC
0.851 0.040 1 171638703 missense variant G/A;C snv 4.0E-06; 7.6E-04 4
rs3788317
TXNRD2
0.851 0.040 22 19902302 intron variant G/T snv 0.30 4
rs4337252
LOXL1
1.000 0.040 15 73934424 intron variant G/C snv 0.52 4
rs7081455 0.851 0.040 10 20349956 upstream gene variant G/A;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
rs7518099
TMCO1-AS1 ; TMCO1
0.925 0.040 1 165767643 intron variant C/T snv 0.89 4
rs7555523
TMCO1
0.925 0.040 1 165749742 intron variant C/A snv 0.88 4
rs75654767
OPTN
0.851 0.040 10 13136766 missense variant G/A snv 3.1E-03 1.0E-03 4
rs7859156
LMX1B
0.851 0.040 9 126637749 intron variant T/C snv 0.74 4
rs786204848
DDX58
0.882 0.040 9 32488884 missense variant C/A snv 4
rs9913911
GAS7
0.925 0.040 17 10127866 intron variant A/G snv 0.32 4
rs10038177
WDR36
0.925 0.040 5 111100751 intron variant C/T snv 0.53 0.54 3
rs12150284
GAS7
1.000 0.040 17 10127773 intron variant C/A;G;T snv 3
rs121909194
MYOC ; MYOCOS
0.882 0.040 1 171636302 missense variant C/G snv 3