Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057517858
rs1057517858
3 0.925 0.240 12 49185714 missense variant C/A;T snv 0.700 0
dbSNP: rs1057518951
rs1057518951
5 0.827 0.160 6 156829296 stop gained C/T snv 0.700 0
dbSNP: rs1057519053
rs1057519053
DCC
2 1.000 0.120 18 52925310 frameshift variant A/- del 0.700 0
dbSNP: rs1057519054
rs1057519054
DCC
2 1.000 0.120 18 53386061 missense variant T/G snv 0.700 0
dbSNP: rs1057519055
rs1057519055
DCC
2 1.000 0.120 18 53386097 missense variant G/A snv 0.700 0
dbSNP: rs1057519056
rs1057519056
DCC
2 1.000 0.120 18 53207746 missense variant G/A;C snv 0.700 0
dbSNP: rs1057519057
rs1057519057
DCC
2 1.000 0.120 18 53391876 missense variant G/A snv 0.700 0
dbSNP: rs1057523157
rs1057523157
3 0.925 0.120 3 47088172 missense variant G/A snv 0.700 0
dbSNP: rs1064796460
rs1064796460
8 0.790 0.400 12 49185197 missense variant C/G;T snv 0.700 0
dbSNP: rs1555155556
rs1555155556
6 0.851 0.120 12 12435627 splice acceptor variant G/T snv 0.700 0
dbSNP: rs1555380716
rs1555380716
5 0.882 0.120 15 34255385 frameshift variant -/C delins 0.700 0
dbSNP: rs1555696625
rs1555696625
7 0.851 0.360 19 13025409 missense variant G/A snv 0.700 0
dbSNP: rs1558519119
rs1558519119
3 0.925 0.120 2 60546061 frameshift variant C/- del 0.700 0
dbSNP: rs1563183469
rs1563183469
3 0.925 0.120 7 70766245 missense variant A/C snv 0.700 0
dbSNP: rs1563406024
rs1563406024
4 0.851 0.240 8 28555799 frameshift variant -/A delins 0.700 0
dbSNP: rs1565627707
rs1565627707
3 0.925 0.240 12 49186657 missense variant C/A snv 0.700 0
dbSNP: rs1569234334
rs1569234334
5 0.851 0.200 X 70329420 missense variant G/T snv 0.700 0
dbSNP: rs1569459580
rs1569459580
2 1.000 0.120 X 111196503 missense variant G/A snv 0.700 0
dbSNP: rs199651452
rs199651452
DCC
2 1.000 0.120 18 53339775 missense variant A/T snv 4.0E-06 0.700 0
dbSNP: rs431905509
rs431905509
8 0.807 0.280 22 19176222 missense variant G/A;C snv 2.0E-05 0.700 0
dbSNP: rs750195040
rs750195040
12 0.827 0.160 9 131506164 inframe deletion CTT/- delins 3.2E-05 7.0E-06 0.700 0
dbSNP: rs754914260
rs754914260
DCC
3 0.925 0.120 18 52923832 stop gained C/A;T snv 4.0E-06 0.700 0
dbSNP: rs775565634
rs775565634
DCC
2 1.000 0.120 18 53339808 missense variant G/A snv 1.5E-04 7.7E-05 0.700 0
dbSNP: rs778139192
rs778139192
14 0.776 0.360 15 89629561 stop gained G/A;T snv 4.1E-06; 7.3E-05 0.700 0
dbSNP: rs782785654
rs782785654
2 1.000 0.120 X 155524537 missense variant G/A snv 5.5E-06 1.9E-05 0.700 0