ClinVar Genomic variation as it relates to human health
GRCh37/hg19 21q22.3(chr21:45995986-46137118)x1
Germline
Classification
(1)
Likely benign
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 | |||
KRTAP10-10 | - | - | - |
GRCh38 GRCh37 |
- | 134 |
KRTAP10-11 | - | - | - |
GRCh38 GRCh37 |
- | 152 |
KRTAP10-12 | - | - | - |
GRCh38 GRCh37 |
- | 140 |
KRTAP10-5 | - | - | - |
GRCh38 GRCh37 |
- | 132 |
KRTAP10-6 | - | - | - |
GRCh38 GRCh37 |
- | 131 |
KRTAP10-7 | - | - | - |
GRCh38 GRCh37 |
- | 136 |
KRTAP10-8 | - | - | - |
GRCh38 GRCh37 |
- | 133 |
KRTAP10-9 | - | - | - |
GRCh38 GRCh37 |
- | 149 |
KRTAP12-1 | - | - | - |
GRCh38 GRCh37 |
- | 114 |
KRTAP12-2 | - | - | - |
GRCh38 GRCh37 |
- | 122 |
There are 3 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 |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
- | RCV000449273.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024