ClinVar Genomic variation as it relates to human health
GRCh38/hg38 1p36.23-36.22(chr1:8283694-12470133)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 | |||
CASZ1 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
392 | 443 | |
MAD2L2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
114 | 173 | |
MFN2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
1243 | 1349 | |
TARDBP | No evidence available | No evidence available |
GRCh38 GRCh37 |
239 | 350 | |
AGTRAP | - | - |
GRCh38 GRCh37 |
17 | 69 | |
ANGPTL7 | - | - |
GRCh38 GRCh37 |
- | 77 | |
C1orf127 | - | - |
GRCh38 GRCh37 |
9 | 58 | |
C1orf167 | - | - | - |
GRCh38 GRCh37 |
- | 62 |
C1orf167-AS1 | - | - | - | GRCh38 | - | 23 |
CA6 | - | - |
GRCh38 GRCh37 |
19 | 63 |
There are 301 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 |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
Dec 22, 2010 | RCV000135807.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024