ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6q23.3(chr6:136630655-137791240)x4
Germline
Classification
(1)
Likely 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 | |||
IFNGR1 | - | - |
GRCh38 GRCh37 |
357 | 376 | |
IL20RA | - | - |
GRCh38 GRCh37 |
25 | 51 | |
IL22RA2 | - | - |
GRCh38 GRCh37 |
19 | 39 | |
LINC02539 | - | - | - |
GRCh38 GRCh37 |
- | 17 |
LINC03004 | - | - | - | GRCh38 | - | 5 |
LOC108169207 | - | - | - | GRCh38 | - | 5 |
LOC111413040 | - | - | - | GRCh38 | - | 5 |
LOC113146415 | - | - | - | GRCh38 | - | 6 |
LOC113146417 | - | - | - | GRCh38 | - | 5 |
LOC123864077 | - | - | - | GRCh38 | - | 6 |
There are 64 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Jul 18, 2014 | RCV000138721.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024