ClinVar Genomic variation as it relates to human health
GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3
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 | |||
EXT1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
956 | 1027 | |
RAD21 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
353 | 414 | |
TRPS1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
590 | 650 | |
ZFPM2 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
62 | 346 | |
KCNK9 | No evidence available | No evidence available |
GRCh38 GRCh37 |
50 | 113 | |
AARD | - | - | - |
GRCh38 GRCh37 |
3 | 57 |
ABRA | - | - |
GRCh38 GRCh37 |
33 | 73 | |
ADCK5 | - | - | - |
GRCh38 GRCh38 GRCh37 |
19 | 92 |
ADCY8 | - | - |
GRCh38 GRCh37 |
48 | 112 | |
ADGRB1 | - | - |
GRCh38 GRCh37 |
58 | 118 |
There are 1398 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) |
|
Nov 30, 2010 | RCV000134353.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023