Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV663739 (NC_000009.12:g.2621564G>A) Homo sapiens

Symbol: CV663739
Name: NC_000009.12:g.2621564G>A
Condition: not provided [RCV000832573]
Clinical Significance: likely benign
Last Evaluated: 06/14/2018
Review Status: criteria provided, single submitter
Related Genes: VLDLR   VLDLR-AS1  
Variant Type: single nucleotide variant (SO:0001483)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.11:g.2621564G>A
NG_012741.1:g.4772G>A
NC_000009.12:g.2621564G>A
NM_003383.3:c.-626G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh3892,621,564 - 2,621,564CLINVAR
GRCh3792,621,564 - 2,621,564CLINVAR
Cytogenetic Map99p24.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14723529
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2020-03-17
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.