ClinVar Genomic variation as it relates to human health
NM_020547.3(AMHR2):c.1332_1358del (p.Gly445_Leu453del)
Germline
Classification
(3)
Pathogenic
criteria provided, multiple submitters, no conflicts
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 | |||
AMHR2 | - | - |
GRCh38 GRCh37 |
111 | 125 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 15, 2009 | RCV000009159.2 | |
Pathogenic (1) |
|
- | RCV002286396.2 | |
Pathogenic (1) |
|
Nov 1, 2022 | RCV002512931.3 |
Citations for germline classification of this variant
HelpText-mined citations for rs764761319 ...
HelpThese citations are identified by LitVar using
the rs number, so they may include citations for more than one variant
at this location. Please review the LitVar results carefully for your
variant of interest.
Record last updated Jun 23, 2024
NCBI staff provided an HGVS expression for allelic variant 600956.0002 from the sequence reported in Figure 3 of the paper by Imbeaud et al., 1996 (PubMed 8872466).