ClinVar Genomic variation as it relates to human health
GRCh37/hg19 7q36.1(chr7:150018908-150591382)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
ACTR3C | - | - | - |
GRCh38 GRCh37 |
21 | 92 |
AOC1 | - | - |
GRCh38 GRCh37 |
48 | 125 | |
GIMAP1 | - | - |
GRCh38 GRCh37 |
- | 87 | |
GIMAP2 | - | - |
GRCh38 GRCh37 |
25 | 101 | |
GIMAP4 | - | - |
GRCh38 GRCh37 |
24 | 97 | |
GIMAP5 | - | - |
GRCh38 GRCh37 |
- | 92 | |
GIMAP6 | - | - |
GRCh38 GRCh37 |
32 | 109 | |
GIMAP7 | - | - |
GRCh38 GRCh37 |
27 | 100 | |
GIMAP8 | - | - |
GRCh38 GRCh37 |
29 | 121 | |
LRRC61 | - | - | - |
GRCh38 GRCh37 |
17 | 93 |
There are 6 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 26, 2021 | RCV002474835.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 31, 2022