ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10q24.32-24.33(chr10:102710547-103110626)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 | |||
ARL3 | - | - |
GRCh38 GRCh37 |
130 | 152 | |
AS3MT | - | - |
GRCh38 GRCh37 |
- | 37 | |
BORCS7 | - | - |
GRCh38 GRCh37 |
- | 24 | |
BORCS7-ASMT | - | - | - | GRCh38 | - | 25 |
CNNM2 | - | - |
GRCh38 GRCh37 |
301 | 376 | |
CYP17A1 | - | - |
GRCh38 GRCh37 |
418 | 545 | |
CYP17A1-AS1 | - | - | - | GRCh38 | - | 100 |
LOC107984265 | - | - | - | GRCh38 | - | 9 |
LOC110408762 | - | - | - | GRCh38 | - | 18 |
LOC121366077 | - | - | - | GRCh38 | - | 7 |
There are 12 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jan 3, 2012 | RCV000138062.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024