ClinVar Genomic variation as it relates to human health
NM_018897.3(DNAH7):c.9920C>G (p.Thr3307Ser)
Germline
Classification
(2)
Benign/Likely benign
criteria provided, multiple submitters, no conflicts
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 | |||
DNAH7 | - | - |
GRCh38 GRCh37 |
358 | 407 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Feb 1, 2023 | RCV003440114.5 | |
DNAH7-related disorder
|
Benign (1) |
|
May 8, 2019 | RCV003929116.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 12, 2024