ClinVar Genomic variation as it relates to human health
GRCh37/hg19 18p11.22(chr18:10535373-10781703)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 | |||
NAPG | - | - |
GRCh38 GRCh37 |
13 | 117 | |
PIEZO2 | - | - |
GRCh38 GRCh37 |
969 | 1090 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 3, 2017 | RCV000683986.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022