ClinVar Genomic variation as it relates to human health
NM_020135.3(WRNIP1):c.449G>T (p.Gly150Val)
Germline
Classification
(1)
Uncertain significance
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 | |||
LOC129995613 | - | - | - | GRCh38 | - | 50 |
MYLK4 | - | - | - |
GRCh38 GRCh37 |
30 | 143 |
WRNIP1 | - | - |
GRCh38 GRCh37 |
25 | 132 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
May 26, 2024 | RCV004685595.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Nov 03, 2024