ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p12-11.2(chr11:40117145-46920718)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 | |||
ALX4 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
278 | 297 | |
EXT2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
754 | 856 | |
PHF21A | Some evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
235 | 253 | |
ACCS | - | - |
GRCh38 GRCh37 |
33 | 54 | |
ACCSL | - | - | - |
GRCh38 GRCh37 |
37 | 58 |
ALKBH3 | - | - |
GRCh38 GRCh37 |
17 | 38 | |
AMBRA1 | - | - |
GRCh38 GRCh37 |
65 | 98 | |
API5 | - | - |
GRCh38 GRCh37 |
8 | 23 | |
ARHGAP1 | - | - |
GRCh38 GRCh37 |
29 | 53 | |
ATG13 | - | - |
GRCh38 GRCh37 |
28 | 52 |
There are 25 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Mar 1, 2021 | RCV001836486.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 17, 2022