ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3q25.1-25.2(chr3:151147204-154845718)
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
AADAC | - | - |
GRCh38 GRCh37 |
- | 48 | |
AADACL2 | - | - | - |
GRCh38 GRCh38 GRCh37 |
9 | 39 |
ARHGEF26 | - | - |
GRCh38 GRCh38 GRCh37 |
61 | 77 | |
DHX36 | - | - |
GRCh38 GRCh38 GRCh37 |
37 | 53 | |
GPR149 | - | - | - |
GRCh38 GRCh37 |
46 | 63 |
IGSF10 | - | - |
GRCh38 GRCh37 |
388 | 417 | |
LINC02877 | - | - | - |
GRCh38 GRCh37 |
- | 18 |
MBNL1 | - | - |
GRCh38 GRCh37 |
14 | 35 | |
MED12L | - | - |
GRCh38 GRCh37 |
148 | 429 | |
MME | - | - |
GRCh38 GRCh37 |
637 | 659 |
There are 3 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) |
|
Mar 1, 2022 | RCV002053377.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 16, 2022