ClinVar Genomic variation as it relates to human health
NM_001005738.1(FPR2):c.*290_*344331dup
Germline
Classification
(1)
not provided
no classification 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 | |||
FPR2 | - | - |
GRCh38 GRCh37 |
23 | 44 | |
FPR3 | - | - |
GRCh38 GRCh37 |
- | 39 | |
LOC125384531 | - | - | - | GRCh38 | - | 10 |
LOC126862921 | - | - | - | GRCh38 | - | 12 |
LOC126862922 | - | - | - | GRCh38 | - | 29 |
LOC126862923 | - | - | - | GRCh38 | - | 11 |
LOC130065045 | - | - | - | GRCh38 | - | 11 |
LOC130065046 | - | - | - | GRCh38 | - | 11 |
LOC130065047 | - | - | - | GRCh38 | - | 11 |
LOC130065048 | - | - | - | GRCh38 | - | 11 |
There are 12 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
not provided (1) |
|
- | RCV000161884.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024