ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q14(chr15:36264417-38045964)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 | |||
MEIS2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
136 | 158 | |
CDIN1 | - | - |
GRCh38 GRCh37 |
95 | 117 | |
LINC02345 | - | - | - | GRCh38 | - | 7 |
LOC110120842 | - | - | - | GRCh38 | - | 8 |
LOC110120858 | - | - | - | GRCh38 | - | 8 |
LOC110120896 | - | - | - | GRCh38 | - | 7 |
LOC110120905 | - | - | - | GRCh38 | - | 7 |
LOC110120936 | - | - | - | GRCh38 | - | 8 |
LOC110120937 | - | - | - | GRCh38 | - | 7 |
LOC121530576 | - | - | - | GRCh38 | - | 8 |
There are 17 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 29, 2016 | RCV000142163.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023