RGD:28901439 Rat Genome Database

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Variant: RGD:28901439 -  Homo sapiens

RGD ID: 28901439
RS ID: rs561326679
ClinVar ID: CV868051
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRP4  LRP4-AS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 46,880,155
GRCh38 11 46,858,604
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002334.4:c.*379C>T
NG_021394.1:g.65019C>T
NC_000011.10:g.46858604G>A
NC_000011.9:g.46880155G>A
More... 		01/17/2018 3 prime utr variant uncertain significance 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_011520103
Location:3UTRS;EXON

Gene Symbol:LRP4
Accession:XM_017017734
Location:3UTRS;EXON

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001104250 CLINVAR
dbSNP (RS) rs561326679 CLINVAR
MedGen C1859309 CLINVAR
NCBI Gene LRP4 CLINVAR
  LRP4-AS1 CLINVAR
OMIM 212780 CLINVAR
  604270 CLINVAR