KCNJ6, potassium inwardly rectifying channel subfamily J member 6, 3763
N. diseases: 104; N. variants: 110
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
21 | 38084132 | intron variant | T/A | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.120 | 21 | 37749345 | intron variant | C/A;T | snv |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
21 | 37739137 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
21 | 38034828 | intron variant | A/T | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 21 | 37714697 | missense variant | C/T | snv |
|
0.800 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
21 | 38112229 | intron variant | G/A | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 21 | 37714645 | missense variant | A/C | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 21 | 37714700 | inframe deletion | GGT/- | delins |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.080 | 21 | 37652469 | intron variant | T/C | snv | 0.26 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37638374 | intron variant | C/A;T | snv | 0.27 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37617262 | 3 prime UTR variant | A/G | snv | 0.32 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37705475 | intron variant | A/G | snv | 0.30 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37681768 | intron variant | G/A | snv | 0.56 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37681654 | intron variant | C/T | snv | 0.50 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37681559 | intron variant | T/A;G | snv | 0.52 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37649639 | intron variant | C/T | snv | 0.31 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37630840 | intron variant | T/C | snv | 0.75 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37710283 | intron variant | C/G;T | snv | 0.28 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37664047 | intron variant | T/A;C | snv |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 21 | 37663909 | intron variant | T/C | snv | 0.57 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37663813 | intron variant | A/C | snv | 0.59 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37663669 | intron variant | A/C | snv | 0.57 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37677171 | intron variant | G/A;C | snv |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 21 | 37665865 | intron variant | T/G | snv | 0.57 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37665503 | intron variant | A/G | snv | 0.57 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 |