ClinVar Genomic variation as it relates to human health
NC_000017.10:g.(?_34892951)_(36104875_?)del
Germline
Classification
(2)
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 | |||
HNF1B | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh38 GRCh37 |
630 | 844 | |
AATF | - | - |
GRCh38 GRCh38 GRCh37 |
47 | 176 | |
ACACA | - | - |
GRCh38 GRCh38 GRCh37 |
260 | 398 | |
C17orf78 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 133 |
DDX52 | - | - |
GRCh38 GRCh38 GRCh37 |
29 | 158 | |
DHRS11 | - | - |
GRCh38 GRCh38 GRCh37 |
22 | 147 | |
DUSP14 | - | - |
GRCh38 GRCh38 GRCh37 |
12 | 139 | |
GGNBP2 | - | - |
GRCh38 GRCh38 GRCh37 |
30 | 159 | |
LHX1 | - | - |
GRCh38 GRCh38 GRCh37 |
28 | 157 | |
MRM1 | - | - |
GRCh38 GRCh38 GRCh37 |
27 | 152 |
There are 3 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) |
|
Oct 3, 2022 | RCV001925612.5 | |
no classifications from unflagged records (1) |
|
- | RCV001943312.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 29, 2024