ClinVar Genomic variation as it relates to human health
GRCh37/hg19 16p13.3(chr16:111043-6627459)x3
Germline
Classification
(1)
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 | |||
CREBBP | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2156 | 2270 | |
PKD1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh38 GRCh37 |
3044 | 3549 | |
TSC2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
10386 | 10575 | |
RBFOX1 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
545 | 698 | |
TPSD1 | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
26 | 91 | |
DNASE1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
36 | 215 | |
MEFV | No evidence available | No evidence available |
GRCh38 GRCh37 |
941 | 1239 | |
SOX8 | No evidence available | No evidence available |
GRCh38 GRCh37 |
62 | 130 | |
ABCA3 | - | - |
GRCh38 GRCh37 |
1517 | 1569 | |
ADCY9 | - | - |
GRCh38 GRCh37 |
73 | 126 |
There are 179 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 |
---|---|---|---|---|
Pathogenic (1) |
|
- | RCV002292215.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023