ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16p13.13(chr16:11466110-12065032)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 | |||
LITAF | No evidence available | No evidence available |
GRCh38 GRCh37 |
279 | 309 | |
BCAR4 | - | - |
GRCh38 GRCh37 |
- | 24 | |
GSPT1 | - | - |
GRCh38 GRCh37 |
11 | 61 | |
RSL1D1 | - | - |
GRCh38 GRCh37 |
22 | 48 | |
SNN | - | - |
GRCh38 GRCh37 |
9 | 32 | |
TNFRSF17 | - | - |
GRCh38 GRCh37 |
- | 43 | |
TXNDC11 | - | - |
GRCh38 GRCh37 |
68 | 92 | |
ZC3H7A | - | - |
GRCh38 GRCh37 |
44 | 69 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 3, 2022 | RCV003485093.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024