DCC, DCC netrin 1 receptor, 1630

N. diseases: 279; N. variants: 101
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057519057
rs1057519057
1.000 0.120 18 53391876 missense variant G/A snv
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1
0.700 0
dbSNP: rs121912967
rs121912967
0.925 0.080 18 52906134 missense variant T/C snv
CUI: C4015970
Disease: ESOPHAGEAL CARCINOMA, SOMATIC
ESOPHAGEAL CARCINOMA, SOMATIC
0.700 0
dbSNP: rs1568364038
rs1568364038
18 53205308 frameshift variant G/- delins
CUI: C1855710
Disease: Bone marrow hypocellularity
Bone marrow hypocellularity
0.700 0
dbSNP: rs199651452
rs199651452
1.000 0.120 18 53339775 missense variant A/T snv 4.0E-06
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1
0.700 0
dbSNP: rs748112308
rs748112308
18 53486808 missense variant G/A snv 1.2E-05 2.8E-05
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1
0.700 0
dbSNP: rs754914260
rs754914260
0.925 0.120 18 52923832 stop gained C/A;T snv 4.0E-06
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1
0.700 0
dbSNP: rs775565634
rs775565634
1.000 0.120 18 53339808 missense variant G/A snv 1.5E-04 7.7E-05
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1
0.700 0
dbSNP: rs797044556
rs797044556
1.000 0.040 18 53486893 frameshift variant TC/- delins
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1
0.700 0
dbSNP: rs1078459
rs1078459
18 53249921 intron variant T/A;C;G snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs10853627
rs10853627
18 53179703 intron variant T/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2018
dbSNP: rs11663156
rs11663156
18 53385388 intron variant T/C snv 0.27
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs1431196
rs1431196
1.000 0.040 18 53305732 intron variant A/G snv 0.31 0.30
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2017 2019
dbSNP: rs6508220
rs6508220
18 53304806 intron variant A/G snv 0.58
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs7245004
rs7245004
18 53190575 intron variant C/A;G snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs10221412
rs10221412
18 53198102 intron variant T/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs10502966
rs10502966
18 53222129 intron variant A/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs11662271
rs11662271
18 53380995 intron variant T/C snv 0.46
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs11665242
rs11665242
18 53380757 intron variant A/G snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1221976
rs1221976
18 52469766 intron variant A/C;G snv
CUI: C0037369
Disease: Smoking
Smoking
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs12607356
rs12607356
18 52917911 intron variant G/A snv 0.39
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs12960505
rs12960505
18 53445812 intron variant G/T snv 0.47
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs13381096
rs13381096
18 53423032 intron variant C/A snv 0.31
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs1367633
rs1367633
18 53221586 intron variant G/A snv 0.36
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1502233
rs1502233
18 53464065 intron variant T/C snv 0.58
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs17411061
rs17411061
18 53268743 intron variant C/T snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018