ClinVar Genomic variation as it relates to human health
NM_000612.6(IGF2):c.306G>A (p.Pro102=)
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 | |||
IGF2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
2 | 182 | |
INS-IGF2 | - | - | - |
GRCh38 GRCh37 |
- | 320 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 19, 2022 | RCV002736751.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 20, 2024