ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19q13.31(chr19:44466919-45029206)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
CEACAM20 | - | - | - |
GRCh38 GRCh37 |
42 | 52 |
ZNF112 | - | - |
GRCh38 GRCh37 |
55 | 65 | |
ZNF155 | - | - |
GRCh38 GRCh37 |
21 | 46 | |
ZNF180 | - | - |
GRCh38 GRCh37 |
44 | 60 | |
ZNF221 | - | - | - |
GRCh38 GRCh37 |
41 | 50 |
ZNF222 | - | - |
GRCh38 GRCh37 |
25 | 35 | |
ZNF223 | - | - | - |
GRCh38 GRCh37 |
38 | 48 |
ZNF224 | - | - |
GRCh38 GRCh37 |
8 | 57 | |
ZNF225 | - | - | - |
GRCh38 GRCh37 |
44 | 55 |
ZNF226 | - | - | - |
GRCh38 GRCh37 |
67 | 79 |
There are 8 more genes 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 20, 2015 | RCV000207290.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 14, 2024