Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs3900940
MYH15
0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs2228315
SELPLG
0.807 0.120 12 108624122 missense variant C/T snv 0.11 0.14 7
rs10890917 11 108988857 intergenic variant C/A;G snv 3.5E-02 1
rs1003346
TMEM245
1.000 9 109053060 intron variant C/A snv 0.43 2
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs218966
PHF14
7 10982603 missense variant A/G snv 0.64 0.68 2
rs9521634
COL4A1
13 110181552 intron variant T/A;C snv 1
rs147270785
MASP2
1.000 0.080 1 11046616 missense variant G/A snv 6.5E-04 6.4E-04 2
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs8103309
SMARCA4
1.000 0.080 19 11064259 intron variant T/C snv 0.40 2
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs12646447 4 110778170 intergenic variant T/C snv 0.15 1
rs1906591 0.851 0.200 4 110787733 intergenic variant G/A snv 0.15 5
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs1906599 4 110791530 upstream gene variant T/C snv 0.67 1
rs13143308 0.882 0.120 4 110793263 upstream gene variant T/C;G snv 4
rs6843082 0.925 0.120 4 110796911 non coding transcript exon variant G/A snv 0.71 3
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs730882079
LDLR
1.000 0.040 19 11105220 missense variant C/T snv 8.0E-06 2
rs121908029
LDLR
0.763 0.200 19 11105588 stop gained G/A;C;T snv 1.6E-05; 1.6E-05; 8.1E-06 13
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17