ClinVar Genomic variation as it relates to human health
GRCh38/hg38 19q13.2-13.31(chr19:42850107-43237158)x1
Germline
Classification
(1)
Benign
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 | |||
LOC284344 | - | - | - | GRCh38 | - | 18 |
PSG1 | - | - |
GRCh38 GRCh37 |
60 | 91 | |
PSG11 | - | - |
GRCh38 GRCh37 |
35 | 69 | |
PSG11-AS1 | - | - | - | GRCh38 | - | 36 |
PSG2 | - | - |
GRCh38 GRCh37 |
44 | 71 | |
PSG4 | - | - |
GRCh38 GRCh37 |
47 | 76 | |
PSG5 | - | - |
GRCh38 GRCh37 |
16 | 63 | |
PSG6 | - | - |
GRCh38 GRCh37 |
58 | 89 | |
PSG7 | - | - |
GRCh38 GRCh37 |
62 | 94 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Oct 19, 2010 | RCV000137003.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024