ClinVar Genomic variation as it relates to human health
GRCh38/hg38 11q22.1(chr11:101139357-101615307)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 | |||
LOC129390347 | - | - | - | GRCh38 | - | 6 |
MIR3920 | - | - | - | GRCh38 | - | 7 |
PGR-AS1 | - | - | - | GRCh38 | - | 6 |
TRPC6 | - | - |
GRCh38 GRCh37 |
415 | 442 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Aug 12, 2011 | RCV000051932.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023