ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16q23.1(chr16:76955286-79080596)x3
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 | |||
ADAMTS18 | - | - |
GRCh38 GRCh37 |
1088 | 1201 | |
CLEC3A | - | - |
GRCh38 GRCh37 |
5 | 76 | |
MON1B | - | - |
GRCh38 GRCh37 |
33 | 91 | |
NUDT7 | - | - |
GRCh38 GRCh37 |
21 | 82 | |
SYCE1L | - | - | - |
GRCh38 GRCh37 |
26 | 85 |
VAT1L | - | - | - |
GRCh38 GRCh37 |
39 | 113 |
WWOX | - | - |
GRCh38 GRCh37 |
883 | 1180 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jan 5, 2018 | RCV000683837.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022