ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q26.1(chr15:89587464-90219354)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 | |||
ABHD2 | - | - |
GRCh38 GRCh37 |
19 | 57 | |
FANCI | - | - |
GRCh38 GRCh37 |
1957 | 2150 | |
KIF7 | - | - |
GRCh38 GRCh37 |
1265 | 1524 | |
LINC00928 | - | - | - |
GRCh38 GRCh37 |
- | 38 |
MIR9-3 | - | - |
GRCh38 GRCh37 |
- | 37 | |
PLIN1 | - | - |
GRCh38 GRCh37 |
96 | 152 | |
POLG | - | - |
GRCh38 GRCh37 |
1 | 2962 | |
RHCG | - | - |
GRCh38 GRCh37 |
34 | 72 | |
RLBP1 | - | - |
GRCh38 GRCh37 |
383 | 423 | |
TICRR | - | - |
GRCh38 GRCh37 |
59 | 182 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
May 2, 2023 | RCV003483246.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024