ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10q26.3(chr10:129293631-129810158)x3
Germline
Classification
(1)
Uncertain significance
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 | |||
LOC107984281 | - | - | - | GRCh38 | - | 40 |
LOC110120892 | - | - | - | GRCh38 | - | 34 |
LOC110120916 | - | - | - | GRCh38 | - | 37 |
LOC121366093 | - | - | - | GRCh38 | - | 36 |
LOC126861093 | - | - | - | GRCh38 | - | 38 |
LOC129390239 | - | - | - | GRCh38 | - | 36 |
LOC130004957 | - | - | - | GRCh38 | - | 37 |
LOC130004958 | - | - | - | GRCh38 | - | 37 |
LOC130004959 | - | - | - | GRCh38 | - | 37 |
LOC130004960 | - | - | - | GRCh38 | - | 37 |
There is 1 more gene 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 8, 2011 | RCV000137637.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024