ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1p31.3(chr1:67544725-67642223)x1
Germline
Classification
(1)
Likely benign
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 | |||
C1orf141 | - | - | - |
GRCh38 GRCh37 |
1 | 27 |
IL23R | - | - |
GRCh38 GRCh37 |
302 | 329 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Nov 30, 2018 | RCV001005101.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022