ClinVar Genomic variation as it relates to human health
GRCh38/hg38 17q24.2(chr17:66424178-66746437)x1
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 | |||
LOC121852945 | - | - | - | GRCh38 | - | 5 |
LOC125316774 | - | - | - | GRCh38 | - | 6 |
LOC125316775 | - | - | - | GRCh38 | - | 6 |
LOC125316776 | - | - | - | GRCh38 | - | 4 |
LOC126862621 | - | - | - | GRCh38 | - | 7 |
LOC129390915 | - | - | - | GRCh38 | - | 6 |
LOC130061470 | - | - | - | GRCh38 | - | 6 |
LOC130061471 | - | - | - | GRCh38 | - | 6 |
LOC130061472 | - | - | - | GRCh38 | - | 4 |
LOC130061473 | - | - | - | GRCh38 | - | 4 |
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 14, 2011 | RCV000137424.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024