ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1p36.11(chr1:27014190-27179034)x3
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 | |||
ARID1A | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1105 | 1283 | |
PIGV | - | - |
GRCh38 GRCh37 |
329 | 338 | |
ZDHHC18 | - | - | - |
GRCh38 GRCh37 |
18 | 37 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV003986851.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024