Source: ALL
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: rs1039528164
rs1039528164
DCC
1 18 53467923 missense variant A/G 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: rs199651452
rs199651452
DCC
2 1.000 0.120 18 53339775 missense variant A/T snv 4.0E-06 0.700 0
dbSNP: rs748112308
rs748112308
DCC ; LINC01917
1 18 53486808 missense variant G/A snv 1.2E-05 2.8E-05 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: rs797044556
rs797044556
DCC ; LINC01917
2 1.000 0.040 18 53486893 frameshift variant TC/- delins 0.700 0