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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 21 | 37665076 | intron variant | A/G | snv | 0.57 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37665202 | intron variant | A/C | snv | 0.57 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37665581 | intron variant | A/G | snv | 0.57 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37665915 | intron variant | G/C | snv | 0.57 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37666591 | intron variant | C/G;T | snv |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 21 | 37666688 | intron variant | C/A;G;T | snv |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 21 | 37677060 | intron variant | A/C;G | snv |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 21 | 37678866 | intron variant | C/A | snv | 0.50 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37680478 | intron variant | G/T | snv | 0.47 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37632199 | intron variant | G/A;T | snv | 0.71 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37614931 | 3 prime UTR variant | T/C | snv | 0.29 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37615595 | 3 prime UTR variant | G/A;C | snv | 0.31 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37616770 | 3 prime UTR variant | G/A | snv | 0.32 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37616885 | 3 prime UTR variant | A/C | snv | 0.26 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37618141 | 3 prime UTR variant | G/A | snv | 0.30 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37618692 | 3 prime UTR variant | A/G | snv | 0.32 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37618732 | 3 prime UTR variant | T/C | snv | 0.25 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37619019 | 3 prime UTR variant | G/C | snv | 0.30 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37638771 | intron variant | C/G;T | snv |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 21 | 37639222 | intron variant | T/C | snv | 0.27 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37640675 | intron variant | T/C | snv | 0.25 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37641826 | intron variant | G/A | snv | 0.27 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37642590 | intron variant | C/A | snv | 0.27 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37643452 | intron variant | T/A | snv | 0.27 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 21 | 37660175 | non coding transcript exon variant | A/G | snv | 0.29 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2012 | 2012 |