ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1p32.3(chr1:51148897-51573845)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 | |||
C1orf185 | - | - | - |
GRCh38 GRCh37 |
3 | 16 |
CDKN2C | - | - |
GRCh38 GRCh37 |
9 | 24 | |
FAF1 | - | - |
GRCh38 GRCh37 |
40 | 57 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Dec 21, 2018 | RCV001005093.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024