ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1q23.1(chr1:156665257-156902706)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 | |||
CRABP2 | - | - |
GRCh38 GRCh37 |
13 | 31 | |
HDGF | - | - |
GRCh38 GRCh37 |
16 | 34 | |
INSRR | - | - |
GRCh38 GRCh37 |
- | 154 | |
ISG20L2 | - | - |
GRCh38 GRCh37 |
26 | 44 | |
LRRC71 | - | - | - |
GRCh38 GRCh37 |
37 | 77 |
METTL25B | - | - | - |
GRCh38 GRCh37 |
40 | 58 |
MRPL24 | - | - |
GRCh38 GRCh37 |
15 | 33 | |
NTRK1 | - | - |
GRCh38 GRCh37 |
1341 | 1528 | |
PEAR1 | - | - |
GRCh38 GRCh37 |
73 | 85 | |
PRCC | - | - |
GRCh38 GRCh37 |
23 | 43 |
There is 1 more gene affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 1, 2021 | RCV001829219.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 17, 2022