ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1p36.33-36.31(chr1:1471075-5831645)
Germline
Classification
(1)
Pathogenic
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 | |||
GNB1 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
300 | 464 | |
SKI | No evidence available | No evidence available |
GRCh38 GRCh37 |
1069 | 1216 | |
TP73 | No evidence available | No evidence available |
GRCh38 GRCh37 |
50 | 161 | |
ACTRT2 | - | - |
GRCh38 GRCh37 |
27 | 167 | |
AJAP1 | - | - |
GRCh38 GRCh37 |
29 | 108 | |
ARHGEF16 | - | - |
GRCh38 GRCh37 |
65 | 179 | |
C1orf174 | - | - | - |
GRCh38 GRCh37 |
5 | 102 |
CALML6 | - | - |
GRCh38 GRCh37 |
9 | 168 | |
CCDC27 | - | - | - |
GRCh38 GRCh37 |
57 | 157 |
CDK11A | - | - |
GRCh38 GRCh37 |
55 | 210 |
There are 33 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) |
|
Nov 1, 2018 | RCV000767773.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023