ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q26.3(chr15:99299033-99997136)x1
Germline
Classification
(1)
Likely 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 | |||
ADAMTS17 | - | - |
GRCh38 GRCh37 |
1196 | 1309 | |
LINC02244 | - | - | - | GRCh38 | - | 34 |
LOC105371017 | - | - | - | GRCh38 | - | 34 |
LOC121847962 | - | - | - | GRCh38 | - | 34 |
LOC121847963 | - | - | - | GRCh38 | - | 35 |
LOC125146367 | - | - | - | GRCh38 | - | 32 |
LOC126862247 | - | - | - | GRCh38 | - | 34 |
LOC129390745 | - | - | - | GRCh38 | - | 30 |
LOC129390746 | - | - | - | GRCh38 | - | 31 |
LOC130058018 | - | - | - | GRCh38 | - | 34 |
There are 20 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
|
Likely benign (1) |
|
Apr 5, 2012 | RCV000137279.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024