ClinVar Genomic variation as it relates to human health
GRCh38/hg38 19q13.41(chr19:51865544-52113443)x3
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 | |||
LOC126862922 | - | - | - | GRCh38 | - | 29 |
LOC126862923 | - | - | - | GRCh38 | - | 11 |
LOC130065045 | - | - | - | GRCh38 | - | 11 |
LOC130065046 | - | - | - | GRCh38 | - | 11 |
LOC130065047 | - | - | - | GRCh38 | - | 11 |
LOC130065048 | - | - | - | GRCh38 | - | 11 |
LOC132090551 | - | - | - | GRCh38 | - | 10 |
ZNF350 | - | - |
GRCh38 GRCh37 |
- | 52 | |
ZNF350-AS1 | - | - | - | GRCh38 | - | 43 |
ZNF432 | - | - |
GRCh38 GRCh37 |
38 | 58 |
There are 8 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
|
Benign (1) |
|
Oct 1, 2010 | RCV000136779.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024