ClinVar Genomic variation as it relates to human health
GRCh38/hg38 1q42.13-44(chr1:230178121-243646135)x1
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 | |||
FH | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1967 | 2051 | |
AKT3 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh38 GRCh37 |
172 | 337 | |
CHRM3 | No evidence available | No evidence available |
GRCh38 GRCh37 |
76 | 147 | |
DISC1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
8 | 167 | |
RYR2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
7381 | 8021 | |
ACTN2 | - | - |
GRCh38 GRCh37 |
1479 | 1539 | |
AGT | - | - |
GRCh38 GRCh37 |
184 | 230 | |
ARID4B | - | - |
GRCh38 GRCh37 |
55 | 109 | |
ARV1 | - | - |
GRCh38 GRCh37 |
41 | 100 | |
B3GALNT2 | - | - |
GRCh38 GRCh38 GRCh37 |
440 | 658 |
There are 361 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 24, 2023 | RCV003327728.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024