ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q26.3(chr15:100455891-101069775)x1
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
ALDH1A3 | - | - |
GRCh38 GRCh37 |
36 | 226 | |
ALDH1A3-AS1 | - | - | - | GRCh38 | - | 134 |
ASB7 | - | - |
GRCh38 GRCh37 |
14 | 111 | |
CERS3 | - | - |
GRCh38 GRCh37 |
85 | 203 | |
GCAWKR | - | - | - | GRCh38 | - | 36 |
LINS1 | - | - |
GRCh38 GRCh37 |
184 | 283 | |
LOC102723335 | - | - | - | GRCh38 | - | 38 |
LOC112272574 | - | - | - | GRCh38 | - | 36 |
LOC121847965 | - | - | - | GRCh38 | - | 36 |
LOC125146368 | - | - | - | GRCh38 | - | 52 |
There are 24 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 |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Aug 12, 2011 | RCV000051973.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023