ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q25.1-25.2(chr15:80955355-82622366)x4
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 | |||
ABHD17C | - | - |
GRCh38 GRCh37 |
7 | 37 | |
CEMIP | - | - |
GRCh38 GRCh37 |
150 | 193 | |
CFAP161 | - | - | - |
GRCh38 GRCh37 |
23 | 45 |
EFL1 | - | - |
GRCh38 GRCh37 |
439 | 469 | |
IL16 | - | - |
GRCh38 GRCh37 |
99 | 128 | |
MESD | - | - |
GRCh38 GRCh37 |
42 | 100 | |
MEX3B | - | - |
GRCh38 GRCh37 |
39 | 60 | |
SAXO2 | - | - | - |
GRCh38 GRCh37 |
26 | 51 |
STARD5 | - | - |
GRCh38 GRCh37 |
6 | 32 | |
TLNRD1 | - | - |
GRCh38 GRCh37 |
32 | 54 |
There is 1 more gene 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) |
|
Jun 30, 2017 | RCV000683713.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022