RGD:11644437 Rat Genome Database

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Variant: RGD:11644437 -  Homo sapiens

RGD ID: 11644437
RS ID: rs886055070
ClinVar ID: CV282638
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRP2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 169,983,951
GRCh38 2 169,127,441
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NG_012634.1:g.240172C>T
NC_000002.12:g.169127441G>A
NC_000002.11:g.169983951G>A
NM_004525.3:c.*1222C>T
More... 		06/14/2016 3 prime utr variant uncertain significance antenatal <1 / 1 000 000 Diaphragmatic hernia exomphalos absent corpus callosum hypertelorism myopia sensorineural deafness and proteinuria; Faciooculoacousticorenal syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LRP2
Accession:NM_004525
Location:3UTRS;EXON

Gene Symbol:LRP2
Accession:XM_047444340
Location:3UTRS;EXON

Gene Symbol:LRP2
Accession:XM_011511183
Location:3UTRS;EXON

Gene Symbol:LRP2
Accession:XM_011511184
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000260176 CLINVAR
dbSNP (RS) rs886055070 CLINVAR
MedGen C1857277 CLINVAR
NCBI Gene LRP2 CLINVAR
OMIM 222448 CLINVAR
  600073 CLINVAR