Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1579050
FMNL2
0.925 0.040 2 152508013 intron variant A/G snv 0.42 3
rs17752199 0.925 0.040 6 51542050 upstream gene variant A/C;G;T snv 3
rs2234926
MYOC
0.882 0.040 1 171652385 missense variant C/T snv 0.15 0.11 3
rs2745572
LOC102723944
0.925 0.040 6 1548134 intergenic variant A/G snv 0.31 3
rs3766355
PTGFR
0.882 0.040 1 78491756 intron variant C/A;T snv 3
rs3858145 0.882 0.040 10 68252081 regulatory region variant A/G snv 0.33 3
rs547984 0.882 0.040 1 237933586 intergenic variant A/C snv 0.60 3
rs6475604
CDKN2B-AS1
0.925 0.040 9 22052735 intron variant T/C snv 0.72 3
rs6478746 0.925 0.040 9 126605119 intron variant G/A snv 0.72 3
rs690037
RFTN1 ; OXNAD1
0.882 0.040 3 16354161 intron variant C/G;T snv 3
rs735860
GCM1
0.882 0.040 6 53258320 regulatory region variant T/C snv 0.66 3
rs74315331
MYOC ; MYOCOS
0.882 0.040 1 171636010 missense variant A/C;T snv 3
rs74315332
MYOCOS ; MYOC
0.882 0.040 1 171636000 missense variant G/T snv 3
rs750460
LOXL1
1.000 0.040 15 73949165 intron variant G/A;T snv 3
rs7854658
LMX1B
0.882 0.040 9 126652659 intron variant G/A snv 0.26 3
rs9853115 0.925 0.040 3 186413811 intergenic variant T/A;G snv 0.51 3
rs10281637 1.000 0.040 7 116511284 downstream gene variant T/C snv 0.28 2
rs1057518844
CREBBP
1.000 0.040 16 3757288 missense variant C/T snv 2
rs10918274
TMCO1
1.000 0.040 1 165745179 intron variant T/C snv 0.89 2
rs11217878
ARHGEF12
1.000 0.040 11 120469674 intron variant G/A snv 0.20 2
rs113985657
EXOC2
1.000 0.040 6 597203 intron variant C/T snv 0.14 2
rs116529882
WDR36
0.925 0.040 5 111110280 missense variant G/A snv 7.5E-04 8.9E-04 2
rs12154178
ESR1
0.925 0.040 6 151929945 intron variant C/A snv 0.59 2
rs121909193
MYOCOS ; MYOC
0.925 0.040 1 171636349 missense variant C/A snv 2
rs12377624
LOC105376277
1.000 0.040 9 126610831 intron variant G/C snv 0.28 2