ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6q22.33(chr6:129591658-129773902)x3
Germline
Classification
(1)
Benign
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 | |||
ARHGAP18 | - | - |
GRCh38 GRCh37 |
42 | 65 | |
LOC113146413 | - | - | - | GRCh38 | - | 7 |
LOC121132706 | - | - | - | GRCh38 | - | 7 |
LOC129389645 | - | - | - | GRCh38 | - | 7 |
LOC129997129 | - | - | - | GRCh38 | - | 7 |
LOC129997130 | - | - | - | GRCh38 | - | 7 |
LOC129997131 | - | - | - | GRCh38 | - | 7 |
LOC129997132 | - | - | - | GRCh38 | - | 7 |
LOC129997133 | - | - | - | GRCh38 | - | 7 |
LOC129997134 | - | - | - | GRCh38 | - | 7 |
There are 4 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Mar 8, 2011 | RCV000136349.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024