Gene: DCC ×
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: rs1078459
rs1078459
DCC
1 18 53249921 intron variant T/A;C;G snv 0.700 1.000 2 2018 2019
dbSNP: rs10853627
rs10853627
DCC
1 18 53179703 intron variant T/A;C snv 0.700 1.000 2 2018 2018
dbSNP: rs11663156
rs11663156
DCC
1 18 53385388 intron variant T/C snv 0.27 0.700 1.000 2 2018 2019
dbSNP: rs1431196
rs1431196
DCC
2 1.000 0.040 18 53305732 intron variant A/G snv 0.31 0.30 0.700 1.000 2 2017 2019
dbSNP: rs6508220
rs6508220
DCC
1 18 53304806 intron variant A/G snv 0.58 0.700 1.000 2 2018 2019
dbSNP: rs7245004
rs7245004
DCC
1 18 53190575 intron variant C/A;G snv 0.700 1.000 2 2018 2019
dbSNP: rs10221412
rs10221412
DCC
1 18 53198102 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10502966
rs10502966
DCC
1 18 53222129 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11662271
rs11662271
DCC
1 18 53380995 intron variant T/C snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs11665242
rs11665242
DCC
1 18 53380757 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs12607356
rs12607356
DCC
1 18 52917911 intron variant G/A snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs12960505
rs12960505
DCC
1 18 53445812 intron variant G/T snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs13381096
rs13381096
DCC
1 18 53423032 intron variant C/A snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs1367633
rs1367633
DCC
1 18 53221586 intron variant G/A snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs1502233
rs1502233
DCC
1 18 53464065 intron variant T/C snv 0.58 0.700 1.000 1 2018 2018
dbSNP: rs17411061
rs17411061
DCC
1 18 53268743 intron variant C/T snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs17417046
rs17417046
DCC
1 18 53458627 intron variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs1972044
rs1972044
DCC
1 18 53404710 intron variant G/A snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs4277413
rs4277413
DCC
2 1.000 0.040 18 53172556 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs4453579
rs4453579
DCC ; LINC01917
1 18 53521463 intron variant G/A snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs62100775
rs62100775
DCC
1 18 53227723 intron variant A/G snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs71367283
rs71367283
DCC
1 18 52525714 intron variant A/C snv 2.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs7506451
rs7506451
DCC
1 18 53044061 intron variant T/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs8083850
rs8083850
DCC
1 18 53180922 intron variant A/G snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs8089865
rs8089865
DCC
4 1.000 0.040 18 53431552 intron variant G/A;C snv 0.700 1.000 1 2018 2018