ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16p13.11-12.3(chr16:15316618-18770833)
Germline
Classification
(1)
Likely pathogenic
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 | |||
MYH11 | No evidence available | No evidence available |
GRCh38 GRCh38 GRCh37 |
2028 | 3792 | |
ABCC1 | - | - |
GRCh38 GRCh38 GRCh37 |
140 | 495 | |
ABCC6 | - | - |
GRCh38 GRCh38 GRCh37 |
1459 | 1822 | |
BMERB1 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 351 |
CEP20 | - | - |
GRCh38 GRCh38 GRCh37 |
19 | 375 | |
MARF1 | - | - |
GRCh38 GRCh38 GRCh37 |
106 | 455 | |
MPV17L | - | - |
GRCh38 GRCh38 GRCh37 |
- | 341 | |
NDE1 | - | - |
GRCh38 GRCh38 GRCh37 |
183 | 1947 | |
NOMO2 | - | - |
GRCh38 GRCh37 |
47 | 91 | |
NOMO3 | - | - |
GRCh38 GRCh38 GRCh37 |
35 | 307 |
There are 2 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely pathogenic (1) |
|
- | RCV002280692.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 10, 2024