ClinVar Genomic variation as it relates to human health
GRCh38/hg38 3q22.1-24(chr3:132716978-144784743)x1
Germline
Classification
(1)
Pathogenic
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 | |||
FOXL2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
231 | 266 | |
ATR | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
3365 | 3463 | |
A4GNT | - | - |
GRCh38 GRCh37 |
21 | 43 | |
AMOTL2 | - | - |
GRCh38 GRCh37 |
62 | 80 | |
ANAPC13 | - | - |
GRCh38 GRCh37 |
4 | 20 | |
ARMC8 | - | - |
GRCh38 GRCh37 |
16 | 44 | |
ATP1B3 | - | - |
GRCh38 GRCh37 |
8 | 27 | |
BFSP2 | - | - |
GRCh38 GRCh37 |
47 | 146 | |
BFSP2-AS1 | - | - | - | GRCh38 | - | 90 |
BPESC1 | - | - | GRCh38 | - | 13 |
There are 293 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Jul 18, 2014 | RCV000143634.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024