Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113624356 0.724 0.400 11 66526181 missense variant T/G snv 1.5E-03 2.1E-03 22
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs1800553 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 17
rs121434491 0.752 0.200 2 55871091 missense variant G/A snv 15
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs137853006 0.776 0.080 4 16013299 missense variant G/A snv 11
rs80338902 0.790 0.200 1 216247118 missense variant C/A snv 9.7E-04 1.3E-03 10
rs1282382243 0.807 0.120 13 50843630 missense variant G/A snv 8
rs768435443 0.807 0.080 1 94055128 missense variant A/G snv 4.0E-06 8
rs201471607 0.851 0.080 1 94046943 missense variant T/C snv 1.4E-04 7.7E-05 7
rs121918284 0.882 0.080 11 61955892 missense variant G/A snv 5.2E-04 3.3E-04 5
rs62638634 0.925 0.080 X 38322921 missense variant C/A snv 4
rs763544450
ERG
1.000 0.080 21 38445560 missense variant T/G snv 4.0E-06 4
rs137853298 0.925 0.080 22 32859351 missense variant A/T snv 3
rs2853502
ND5 ; CYTB
1.000 0.200 MT 13276 missense variant A/C;G;T snv 2
rs774038422
ERG
1.000 0.080 21 38391009 missense variant C/T snv 4.0E-06 7.0E-06 2
rs375090109 6 42722120 missense variant C/A;G snv 4.0E-06; 2.4E-05 1
rs773223321 4 89935190 missense variant G/A snv 1.6E-05 1
rs3825172 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 14
rs74421874 0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14
rs2146323 0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs735286 6 43776884 non coding transcript exon variant C/T snv 0.23 1
rs771676129 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs999947969 0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82