ClinVar Genomic variation as it relates to human health
GRCh37/hg19 2q13(chr2:113735617-113891118)x1
Germline
Classification
(1)
Benign
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 |
13 | 36 | |
IL1RN | - | - |
GRCh38 GRCh37 |
225 | 248 | |
IL36A | - | - |
GRCh38 GRCh37 |
17 | 40 | |
IL36B | - | - |
GRCh38 GRCh37 |
9 | 32 | |
IL36G | - | - |
GRCh38 GRCh37 |
14 | 37 | |
IL36RN | - | - |
GRCh38 GRCh37 |
192 | 215 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
- | RCV000448884.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024