ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1p35.2(chr1:31766058-31921862)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 | |||
FABP3 | - | - |
GRCh38 GRCh37 |
14 | 29 | |
SERINC2 | - | - |
GRCh38 GRCh37 |
34 | 68 | |
SNRNP40 | - | - |
GRCh38 GRCh37 |
13 | 33 | |
ZCCHC17 | - | - |
GRCh38 GRCh37 |
8 | 23 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 1, 2021 | RCV001827729.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 17, 2022