Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913026
ERCC2
0.851 0.400 19 45352235 missense variant G/A snv 2.4E-05 9.1E-05 3
rs376556895
ERCC2
0.851 0.400 19 45352801 missense variant C/G;T snv 1.5E-04; 8.0E-06 3
rs41556519
ERCC2
0.807 0.400 19 45352352 missense variant G/A snv 6.0E-05 2.8E-05 3
rs121913020
ERCC2
0.882 0.160 19 45368655 missense variant C/T snv 2.0E-05 6.3E-05 2
rs762309206
ERCC2
0.925 0.160 19 45364833 splice donor variant CACT/- delins 1.1E-04 2
rs121913018
ERCC2
1.000 0.080 19 45352226 missense variant C/G snv 2.0E-05 4.2E-05 1
rs121913021
ERCC2
0.882 0.160 19 45352580 missense variant G/A snv 2.8E-05 4.2E-05 1
rs121913022
ERCC2
1.000 0.080 19 45352262 missense variant C/G snv 1.4E-05 1
rs768342562
MPLKIP ; SUGCT
1.000 0.080 7 40133093 frameshift variant -/T delins 4.0E-06 1