ClinVar Genomic variation as it relates to human health
GRCh38/hg38 8p12(chr8:30368765-36421541)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 | |||
DUSP26 | - | - |
GRCh38 GRCh37 |
5 | 72 | |
FUT10 | - | - |
GRCh38 GRCh37 |
26 | 94 | |
GSR | - | - |
GRCh38 GRCh37 |
127 | 229 | |
GTF2E2 | - | - |
GRCh38 GRCh37 |
136 | 215 | |
LINC01288 | - | - | - | GRCh38 | - | 32 |
LOC101929550 | - | - | - | GRCh38 | - | 37 |
LOC105379362 | - | - | - | GRCh38 | - | 34 |
LOC108004525 | - | - | - | GRCh38 | - | 38 |
LOC110121192 | - | - | - | GRCh38 | - | 32 |
LOC113788276 | - | - | - | GRCh38 | - | 38 |
There are 75 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 27, 2013 | RCV000139926.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024