ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10p13(chr10:15680938-16480748)x3
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
ITGA8 | - | - |
GRCh38 GRCh37 |
316 | 340 | |
LINC02654 | - | - | - | GRCh38 | - | 9 |
LOC121366044 | - | - | - | GRCh38 | - | 9 |
LOC129390137 | - | - | - | GRCh38 | - | 8 |
LOC129390138 | - | - | - | GRCh38 | - | 9 |
LOC129390139 | - | - | - | GRCh38 | - | 8 |
LOC130003434 | - | - | - | GRCh38 | - | 9 |
LOC130003435 | - | - | - | GRCh38 | - | 9 |
LOC130003436 | - | - | - | GRCh38 | - | 9 |
LOC130003437 | - | - | - | GRCh38 | - | 9 |
There are 3 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
|
Uncertain significance (1) |
|
Aug 12, 2011 | RCV000051623.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023