ClinVar Genomic variation as it relates to human health
GRCh38/hg38 6q27(chr6:167963663-168157303)x3
Germline
Classification
(1)
Benign
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 | |||
AFDN | - | - |
GRCh38 GRCh37 |
18 | 86 | |
FRMD1 | - | - | - |
GRCh38 GRCh37 |
75 | 146 |
HGC6.3 | - | - | - | GRCh38 | - | 28 |
KIF25 | - | - |
GRCh38 GRCh37 |
40 | 110 | |
KIF25-AS1 | - | - | - | GRCh38 | - | 28 |
LOC126859899 | - | - | - | GRCh38 | - | 28 |
LOC129389722 | - | - | - | GRCh38 | - | 28 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Aug 12, 2011 | RCV000148243.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024