ClinVar Genomic variation as it relates to human health
GRCh37/hg19 12q24.31(chr12:123807132-124300075)x3
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 | |||
ATP6V0A2 | - | - |
GRCh38 GRCh37 |
610 | 716 | |
DDX55 | - | - | - |
GRCh38 GRCh37 |
49 | 77 |
DNAH10 | - | - |
GRCh38 GRCh38 GRCh37 |
437 | 547 | |
EIF2B1 | - | - |
GRCh38 GRCh37 |
231 | 322 | |
GTF2H3 | - | - |
GRCh38 GRCh37 |
6 | 42 | |
KMT5A | - | - |
GRCh38 GRCh37 |
4 | 36 | |
RILPL1 | - | - |
GRCh38 GRCh37 |
14 | 53 | |
RILPL2 | - | - |
GRCh38 GRCh37 |
13 | 45 | |
SBNO1 | - | - |
GRCh38 GRCh37 |
54 | 86 | |
SNRNP35 | - | - |
GRCh38 GRCh37 |
20 | 57 |
There are 2 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 9, 2020 | RCV001834350.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022