rs6662343 Rat Genome Database

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Variant: rs6662343 -  Homo sapiens

RGD ID: 11587578
RS ID: rs6662343
ClinVar ID: CV279600
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LEFTY2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 226,124,912
GRCh38 1 225,937,212
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003240.5:c.*229C>T
NG_008118.1:g.9009C>T
NC_000001.11:g.225937212G>A
NC_000001.10:g.226124912G>A
More...
04/28/2017 3 prime utr variant likely benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LEFTY2
Accession:NM_003240
Location:3UTRS;EXON

Gene Symbol:LEFTY2
Accession:XM_011544266
Location:3UTRS;EXON

Gene Symbol:LEFTY2
Accession:NM_001172425
Location:3UTRS;EXON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000296054 CLINVAR
  RCV004710769 CLINVAR
dbSNP (RS) rs6662343 CLINVAR
MedGen C1866091 CLINVAR
  C3661900 CLINVAR
NCBI Gene LEFTY2 CLINVAR
OMIM 601877 CLINVAR