ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6p22.2(chr6:25991391-26116829)x3
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 | |||
H1-1 | - | - |
GRCh38 GRCh37 |
10 | 22 | |
H1-2 | - | - |
GRCh38 GRCh37 |
6 | 30 | |
H1-6 | - | - |
GRCh38 GRCh37 |
17 | 34 | |
H2AC4 | - | - |
GRCh38 GRCh37 |
9 | 22 | |
H2BC3 | - | - |
GRCh38 GRCh37 |
8 | 21 | |
H2BC4 | - | - |
GRCh38 GRCh37 |
- | 18 | |
H3C1 | - | - |
GRCh38 GRCh37 |
4 | 17 | |
H3C2 | - | - |
GRCh38 GRCh37 |
2 | 17 | |
H3C3 | - | - |
GRCh38 GRCh37 |
1 | 16 | |
H4C1 | - | - |
GRCh38 GRCh37 |
1 | 14 |
There are 22 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 |
---|---|---|---|---|
Likely benign (1) |
|
Apr 30, 2011 | RCV000140950.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023