ClinVar Genomic variation as it relates to human health
GRCh37/hg19 20q13.33(chr20:62766314-62915555)x1
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 | |||
MYT1 | - | - |
GRCh38 GRCh38 GRCh37 |
118 | 170 | |
PCMTD2 | - | - | - |
GRCh38 GRCh38 GRCh37 |
14 | 63 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 22, 2018 | RCV000684102.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022