ClinVar Genomic variation as it relates to human health
GRCh37/hg19 17q24.2-24.3(chr17:65343022-69344022)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 | |||
BPTF | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
670 | 718 | |
ABCA10 | - | - |
GRCh38 GRCh37 |
92 | 108 | |
ABCA5 | - | - |
GRCh38 GRCh37 |
142 | 156 | |
ABCA6 | - | - |
GRCh38 GRCh37 |
102 | 119 | |
ABCA8 | - | - |
GRCh38 GRCh37 |
102 | 116 | |
ABCA9 | - | - |
GRCh38 GRCh37 |
87 | 114 | |
AMZ2 | - | - |
GRCh38 GRCh37 |
29 | 42 | |
ARSG | - | - |
GRCh38 GRCh37 |
315 | 464 | |
C17orf58 | - | - | - |
GRCh38 GRCh37 |
- | 16 |
FAM20A | - | - |
GRCh38 GRCh37 |
97 | 246 |
There are 10 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV000446484.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024