ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1q23.1(chr1:158489545-158901383)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 | |||
MNDA | - | - |
GRCh38 GRCh37 |
544 | 560 | |
OR10X1 | - | - | - |
GRCh38 GRCh37 |
24 | 35 |
OR10Z1 | - | - | - |
GRCh38 GRCh37 |
17 | 73 |
OR6K2 | - | - | - |
GRCh38 GRCh37 |
34 | 46 |
OR6K3 | - | - | - |
GRCh38 GRCh37 |
31 | 46 |
OR6K6 | - | - | - |
GRCh38 GRCh37 |
20 | 35 |
OR6N1 | - | - | - |
GRCh38 GRCh37 |
21 | 56 |
OR6N2 | - | - | - |
GRCh38 GRCh37 |
- | 34 |
OR6P1 | - | - | - |
GRCh38 GRCh37 |
30 | 41 |
OR6Y1 | - | - | - |
GRCh38 GRCh37 |
25 | 36 |
There are 2 more genes 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) |
|
Sep 25, 2017 | RCV000684663.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022