ClinVar Genomic variation as it relates to human health
NC_000010.10:g.(?_102987027)_(103384587_?)dup
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
BTRC | No evidence available | No evidence available |
GRCh38 GRCh37 |
73 | 131 | |
FBXW4 | No evidence available | No evidence available |
GRCh38 GRCh37 |
70 | 148 | |
LBX1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
15 | 52 | |
POLL | No evidence available | No evidence available |
GRCh38 GRCh37 |
60 | 112 | |
DPCD | - | - |
GRCh38 GRCh37 |
15 | 71 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 13, 2023 | RCV003109856.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 17, 2024