ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10p11.21(chr10:34891282-35211554)
Germline
Classification
(1)
Likely 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 | |||
CREM | - | - |
GRCh38 GRCh37 |
14 | 37 | |
CUL2 | - | - |
GRCh38 GRCh37 |
33 | 56 | |
LOC129390164 | - | - | - | GRCh38 | - | 8 |
LOC129390165 | - | - | - | GRCh38 | - | 8 |
LOC130003671 | - | - | - | GRCh38 | - | 7 |
LOC130003672 | - | - | - | GRCh38 | - | 7 |
LOC130003673 | - | - | - | GRCh38 | - | 7 |
LOC130003674 | - | - | - | GRCh38 | - | 7 |
LOC130003675 | - | - | - | GRCh38 | - | 7 |
LOC130003676 | - | - | - | GRCh38 | - | 6 |
There are 5 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
- | RCV003883259.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 11, 2024