ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p15.4(chr11:6801941-7136661)x3
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 | |||
NLRP14 | - | - |
GRCh38 GRCh37 |
146 | 211 | |
OR10A2 | - | - | - |
GRCh38 GRCh37 |
24 | 45 |
OR10A4 | - | - | - |
GRCh38 GRCh37 |
20 | 41 |
OR10A5 | - | - |
GRCh38 GRCh37 |
16 | 36 | |
OR2AG1 | - | - | - |
GRCh38 GRCh37 |
28 | 46 |
OR2D2 | - | - |
GRCh38 GRCh37 |
28 | 50 | |
OR2D3 | - | - | - |
GRCh38 GRCh37 |
24 | 46 |
OR6A2 | - | - |
GRCh38 GRCh37 |
28 | 46 | |
RBMXL2 | - | - |
GRCh38 GRCh37 |
- | 62 | |
ZNF214 | - | - |
GRCh38 GRCh37 |
28 | 49 |
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) |
|
Jan 1, 2023 | RCV003484831.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024