ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19q13.43(chr19:58026985-58255427)x3
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 | |||
ZIK1 | - | - | - |
GRCh38 GRCh37 |
31 | 56 |
ZNF134 | - | - |
GRCh38 GRCh37 |
36 | 62 | |
ZNF154 | - | - |
GRCh38 GRCh37 |
32 | 58 | |
ZNF211 | - | - |
GRCh38 GRCh37 |
29 | 60 | |
ZNF416 | - | - | - |
GRCh38 GRCh37 |
27 | 52 |
ZNF530 | - | - | - |
GRCh38 GRCh37 |
27 | 52 |
ZNF549 | - | - | - |
GRCh38 GRCh37 |
36 | 59 |
ZNF550 | - | - | - |
GRCh38 GRCh37 |
- | 25 |
ZNF551 | - | - | - |
GRCh38 GRCh37 |
43 | 70 |
ZNF671 | - | - | - |
GRCh38 GRCh37 |
32 | 59 |
There is 1 more gene affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Mar 1, 2021 | RCV001832942.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022