ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q22.1(chr7:98396469-102108193)x1
Germline
Classification
(1)
Likely pathogenic
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 | |||
TRRAP | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1656 | 1732 | |
CYP3A43 | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
29 | 56 | |
ACHE | - | - |
GRCh38 GRCh37 |
34 | 58 | |
ACTL6B | - | - |
GRCh38 GRCh37 |
114 | 140 | |
AGFG2 | - | - |
GRCh38 GRCh37 |
30 | 57 | |
ALKBH4 | - | - |
GRCh38 GRCh37 |
35 | 57 | |
AP1S1 | - | - |
GRCh38 GRCh37 |
56 | 162 | |
AP4M1 | - | - |
GRCh38 GRCh37 |
405 | 493 | |
ARPC1A | - | - |
GRCh38 GRCh37 |
18 | 41 | |
ARPC1B | - | - |
GRCh38 GRCh37 |
292 | 318 |
There are 85 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 |
---|---|---|---|---|
Likely pathogenic (1) |
|
- | RCV003986701.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024