LINGO1, leucine rich repeat and Ig domain containing 1, 84894
N. diseases: 44; N. variants: 22
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
15 | 77720276 | intron variant | C/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 77720346 | intron variant | G/A | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.827 | 0.120 | 15 | 77680428 | intron variant | C/T | snv | 0.42 |
|
0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
15 | 77741926 | intron variant | T/C | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
15 | 77742361 | intron variant | C/T | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
15 | 77768444 | intron variant | G/A | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 15 | 77615044 | missense variant | T/C | snv | 1.2E-05 |
|
0.800 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 15 | 77615038 | missense variant | C/T | snv | 2.8E-05 |
|
0.800 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
15 | 77741926 | intron variant | T/C | snv | 0.37 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.040 | 15 | 77727790 | intron variant | A/G | snv | 0.35 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.827 | 0.120 | 15 | 77680428 | intron variant | C/T | snv | 0.42 |
|
Immune System Diseases; Nervous System Diseases | 0.010 | < 0.001 | 1 | 2013 | 2013 | |||||||
|
0.851 | 0.080 | 15 | 77671545 | intron variant | A/G | snv | 0.28 |
|
Immune System Diseases; Nervous System Diseases | 0.010 | < 0.001 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.040 | 15 | 77788395 | non coding transcript exon variant | C/G | snv | 0.56 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.040 | 15 | 77809567 | intron variant | A/G | snv | 0.47 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.040 | 15 | 77809567 | intron variant | A/G | snv | 0.47 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.040 | 15 | 77727790 | intron variant | A/G | snv | 0.35 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 15 | 77775291 | intron variant | C/T | snv | 0.35 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.040 | 15 | 77714500 | intron variant | T/C | snv | 0.50 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.040 | 15 | 77714500 | intron variant | T/C | snv | 0.50 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.040 | 15 | 77771243 | intron variant | A/C | snv | 0.19 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 15 | 77740365 | intron variant | G/A | snv | 0.11 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 15 | 77772882 | intron variant | G/A;T | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 15 | 77745782 | intron variant | A/C;T | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 15 | 77756650 | intron variant | C/A;T | snv | 0.20 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.851 | 0.080 | 15 | 77671545 | intron variant | A/G | snv | 0.28 |
|
Nervous System Diseases | 0.900 | 0.714 | 14 | 2009 | 2016 |