ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16q23.1(chr16:77075284-78151019)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 | |||
ADAMTS18 | - | - |
GRCh38 GRCh37 |
1078 | 1189 | |
CLEC3A | - | - |
GRCh38 GRCh37 |
5 | 75 | |
MON1B | - | - |
GRCh38 GRCh37 |
30 | 88 | |
NUDT7 | - | - |
GRCh38 GRCh37 |
17 | 77 | |
SYCE1L | - | - |
GRCh38 GRCh37 |
23 | 82 | |
VAT1L | - | - |
GRCh38 GRCh37 |
34 | 107 | |
WWOX | - | - |
GRCh38 GRCh37 |
868 | 1160 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 6, 2022 | RCV003485128.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024