ClinVar Genomic variation as it relates to human health
NC_000019.9:g.(?_589946)_(5696788_?)dup
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
STK11 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2368 | 2642 | |
ELANE | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh38 GRCh37 |
549 | 591 | |
MAP2K2 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
770 | 851 | |
GRIN3B | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
119 | 160 | |
ABCA7 | - | - |
GRCh38 GRCh37 |
292 | 338 | |
ABHD17A | - | - |
GRCh38 GRCh37 |
19 | 53 | |
ADAMTSL5 | - | - | - |
GRCh38 GRCh37 |
50 | 80 |
ADAT3 | - | - |
GRCh38 GRCh37 |
- | 141 | |
AMH | - | - |
GRCh38 GRCh37 |
140 | 185 | |
ANKRD24 | - | - |
GRCh38 GRCh37 |
87 | 113 |
There are 143 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 10, 2022 | RCV003113597.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 10, 2024