ClinVar Genomic variation as it relates to human health
NC_000017.10:g.(?_29421945)_(29509683_?)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 | |||
NF1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh38 GRCh37 |
13560 | 13967 | |
LOC108281169 | - | - | - |
GRCh38 GRCh38 |
- | 30 |
LOC108281170 | - | - | - |
GRCh38 GRCh38 |
- | 34 |
LOC108281180 | - | - | - |
GRCh38 GRCh38 |
- | 36 |
LOC111811965 | - | - | - |
GRCh38 GRCh38 |
- | 187 |
MIR4733HG | - | - | - |
GRCh38 GRCh38 |
- | 198 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Oct 1, 2016 | RCV000462709.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023