ClinVar Genomic variation as it relates to human health
GRCh38/hg38 20q11.23-12(chr20:38912733-39376861)x1
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 | |||
DHX35 | - | - | - |
GRCh38 GRCh37 |
37 | 45 |
FAM83D | - | - |
GRCh38 GRCh37 |
5 | 16 | |
LINC01734 | - | - | - | GRCh38 | - | 4 |
LOC110121317 | - | - | - | GRCh38 | - | 4 |
LOC112694710 | - | - | - | GRCh38 | - | 4 |
LOC126863027 | - | - | - | GRCh38 | - | 4 |
LOC129391176 | - | - | - | GRCh38 | - | 4 |
LOC130065864 | - | - | - | GRCh38 | - | 4 |
LOC130065865 | - | - | - | GRCh38 | - | 6 |
LOC130065866 | - | - | - | GRCh38 | - | 4 |
There are 4 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) |
|
Oct 7, 2011 | RCV000137608.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024