rs886046059 Rat Genome Database

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Variant: rs886046059 -  Homo sapiens

RGD ID: 11662180
RS ID: rs886046059
ClinVar ID: CV280896
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 226,129,062
GRCh38 1 225,941,362
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.225941362G>T
NM_003240.3:c.-222C>A
NC_000001.10:g.226129062G>T
NM_003240.4:c.-222C>A
More...
06/14/2016 5 prime utr variant uncertain significance Heterotaxia; Heterotaxy syndrome
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Heterotaxy  (IAGP)

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000383720 CLINVAR
dbSNP (RS) rs886046059 CLINVAR
MedGen C3178805 CLINVAR
NCBI Gene LEFTY2 CLINVAR
OMIM 601877 CLINVAR