Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs104894833
RPL36A-HNRNPH2 ; GLA
0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1317947
MMP20 ; LOC101928477
1.000 0.080 11 102617342 intron variant G/A snv 0.41 2
rs1423621991
MMP1 ; WTAPP1
11 102796745 missense variant C/T snv 1
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs2282377
ASPG
1.000 0.080 14 104105483 intron variant C/G snv 0.12 0.12 2
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 5
rs1556446493
COL4A5
X 108668328 missense variant G/T snv 3
rs1933182 1.000 0.080 1 109457216 intergenic variant A/C snv 0.63 3
rs2208338
ELOVL2
1.000 0.080 6 11028421 intron variant G/A snv 0.21 2
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs12194000
SLC22A16
1.000 0.080 6 110454809 intron variant A/G;T snv 2
rs10794720
WDR37
1.000 0.080 10 1110225 intron variant T/C snv 0.89 4
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs2230774
ROCK2
0.807 0.240 2 11218994 missense variant G/C;T snv 0.49 12
rs2074388
ALPK1
1.000 4 112431241 missense variant G/A snv 0.62 0.65 3
rs2074379
ALPK1
1.000 4 112431743 missense variant G/A snv 0.62 0.65 3
rs2074380
ALPK1
4 112432155 missense variant G/A;T snv 8.5E-03; 2.4E-05 2
rs2074381
ALPK1
4 112432293 missense variant A/G snv 8.5E-03 5.5E-03 2
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs6046
F7
0.925 0.080 13 113118845 missense variant G/A;C;T snv 0.13 5
rs814698
ZNF618
1.000 0.080 9 113967563 intron variant A/T snv 0.22 2