ClinVar Genomic variation as it relates to human health
GRCh38/hg38 3p25.1(chr3:15806288-16201982)x3
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 | |||
ANKRD28 | - | - |
GRCh38 GRCh37 |
12 | 84 | |
GALNT15 | - | - |
GRCh38 GRCh37 |
61 | 87 | |
LOC112935902 | - | - | - | GRCh38 | - | 10 |
LOC121725131 | - | - | - | GRCh38 | - | 10 |
LOC126806618 | - | - | - | GRCh38 | - | 10 |
LOC129936284 | - | - | - | GRCh38 | - | 10 |
LOC129936285 | - | - | - | GRCh38 | - | 10 |
LOC129936286 | - | - | - | GRCh38 | - | 10 |
LOC129936287 | - | - | - | GRCh38 | - | 10 |
LOC129936288 | - | - | - | GRCh38 | - | 10 |
There are 2 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 |
---|---|---|---|---|
Likely benign (1) |
|
Apr 30, 2011 | RCV000140994.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023