ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q22.1(chr10:73321269-74612651)x1
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 | |||
ANAPC16 | - | - |
GRCh38 GRCh37 |
4 | 19 | |
ASCC1 | - | - |
GRCh38 GRCh37 |
181 | 197 | |
C10orf105 | - | - | - |
GRCh38 GRCh37 |
- | 510 |
CDH23 | - | - |
GRCh38 GRCh37 |
4669 | 5506 | |
CHST3 | - | - |
GRCh38 GRCh37 |
467 | 486 | |
DDIT4 | - | - |
GRCh38 GRCh37 |
11 | 31 | |
DNAJB12 | - | - |
GRCh38 GRCh37 |
12 | 31 | |
MCU | - | - |
GRCh38 GRCh37 |
9 | 32 | |
MICU1 | - | - |
GRCh38 GRCh37 |
295 | 311 | |
PSAP | - | - |
GRCh38 GRCh37 |
865 | 922 |
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) |
|
Aug 12, 2022 | RCV003483098.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024