ClinVar Genomic variation as it relates to human health
NC_000002.12:g.(?_112924872)_(113105404_?)del
Germline
Classification
(1)
Uncertain significance
no assertion criteria provided
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 | |||
IL1F10 | - | - |
GRCh38 GRCh37 |
9 | 32 | |
IL1RN | - | - |
GRCh38 GRCh37 |
221 | 244 | |
IL36A | - | - |
GRCh38 GRCh37 |
9 | 31 | |
IL36B | - | - |
GRCh38 GRCh37 |
6 | 28 | |
IL36G | - | - |
GRCh38 GRCh37 |
6 | 28 | |
IL36RN | - | - |
GRCh38 GRCh37 |
189 | 212 | |
LOC112806039 | - | - | - | GRCh38 | - | 2 |
LOC122817730 | - | - | - | GRCh38 | - | 3 |
LOC126806315 | - | - | - | GRCh38 | - | 2 |
LOC129934600 | - | - | - | GRCh38 | - | 3 |
There are 3 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Oct 20, 2021 | RCV001824107.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023