ClinVar Genomic variation as it relates to human health
GRCh38/hg38 5q35.3(chr5:180581319-180846638)x3
Germline
Classification
(1)
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 | |||
FLT4 | - | - |
GRCh38 GRCh37 |
328 | 401 | |
HEIH | - | - | GRCh38 | - | 12 | |
LINC00847 | - | - | - | GRCh38 | - | 12 |
LINC02222 | - | - | - | GRCh38 | - | 12 |
LOC123575638 | - | - | - | GRCh38 | - | 12 |
LOC123575639 | - | - | - | GRCh38 | - | 12 |
LOC126807632 | - | - | - | GRCh38 | - | 46 |
LOC129995471 | - | - | - | GRCh38 | - | 12 |
LOC129995472 | - | - | - | GRCh38 | - | 12 |
LOC129995473 | - | - | - | GRCh38 | - | 12 |
There are 8 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 |
---|---|---|---|---|
Benign (1) |
|
Oct 14, 2010 | RCV000135917.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023