RGD:11603723 Rat Genome Database

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Variant: RGD:11603723 -  Homo sapiens

RGD ID: 11603723
RS ID: rs774819807
ClinVar ID: CV320771
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRP4  LRP4-AS1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 46,878,948
GRCh38 11 46,857,397
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_021394.1:g.66226T>G
NC_000011.10:g.46857397A>C
NC_000011.9:g.46878948A>C
NM_002334.3:c.*1586T>G
More... 		06/14/2016 3 prime utr variant uncertain significance infancy <1 / 1 000 000 Cenani syndactylism; Syndactyly Cenani Lenz type; Syndactyly type 7; SYNDACTYLY, TYPE VII
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LRP4
Accession:XM_017017734
Location:3UTRS;EXON

Gene Symbol:LRP4
Accession:XM_011520104
Location:3UTRS;EXON

Gene Symbol:LRP4
Accession:NM_002334
Location:3UTRS;EXON

Gene Symbol:LRP4
Accession:XM_011520103
Location:3UTRS;EXON

Gene Symbol:LRP4-AS1
Accession:NR_038909
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000302929 CLINVAR
dbSNP (RS) rs774819807 CLINVAR
MedGen C1859309 CLINVAR
NCBI Gene LRP4 CLINVAR
  LRP4-AS1 CLINVAR
OMIM 212780 CLINVAR
  604270 CLINVAR