ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3q29(chr3:197386179-197851986)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 | |||
FYTTD1 | - | - |
GRCh38 GRCh37 |
13 | 74 | |
IQCG | - | - |
GRCh38 GRCh37 |
23 | 202 | |
LMLN | - | - |
GRCh38 GRCh37 |
27 | 85 | |
LRCH3 | - | - | - |
GRCh38 GRCh37 |
68 | 134 |
RPL35A | - | - |
GRCh38 GRCh37 |
- | 172 | |
RUBCN | - | - |
GRCh38 GRCh37 |
121 | 182 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 19, 2018 | RCV000849416.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022