ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q21.13(chr7:89998146-90352986)
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 | |||
CFAP69 | - | - |
GRCh38 GRCh37 |
85 | 120 | |
FAM237B | - | - | - | GRCh38 | - | 6 |
GTPBP10 | - | - |
GRCh38 GRCh37 |
22 | 42 | |
LOC101927446 | - | - | - | GRCh38 | - | 6 |
LOC129998766 | - | - | - | GRCh38 | - | 15 |
LOC129998767 | - | - | - | GRCh38 | - | 15 |
LOC129998768 | - | - | - | GRCh38 | - | 15 |
LOC129998769 | - | - | - | GRCh38 | - | 15 |
LOC129998770 | - | - | - | GRCh38 | - | 6 |
LOC129998771 | - | - | - | GRCh38 | - | 7 |
There are 3 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Jan 27, 2022 | RCV001823081.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jul 29, 2024