ClinVar Genomic variation as it relates to human health
NC_000017.10:g.(?_27573882)_(29576157_?)del
Germline
Classification
(1)
Pathogenic
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 |
13562 | 13969 | |
TAOK1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
153 | 166 | |
CRYBA1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
68 | 82 | |
RNF135 | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
87 | 147 | |
SLC6A4 | No evidence available | No evidence available |
GRCh38 GRCh37 |
124 | 144 | |
ABHD15 | - | - |
GRCh38 GRCh37 |
24 | 45 | |
ADAP2 | - | - |
GRCh38 GRCh38 GRCh37 |
20 | 80 | |
ANKRD13B | - | - |
GRCh38 GRCh37 |
26 | 37 | |
ATAD5 | - | - |
GRCh38 GRCh37 |
120 | 179 | |
BLMH | - | - |
GRCh38 GRCh37 |
17 | 30 |
There are 13 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 |
---|---|---|---|---|
Pathogenic (1) |
|
May 19, 2022 | RCV003109263.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Nov 11, 2023