rs11227515 Rat Genome Database

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Variant: rs11227515 -  Homo sapiens

RGD ID: 150501542
RS ID: rs11227515
ClinVar ID: CV1256325
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BBS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 66,287,383
GRCh38 11 66,519,912
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_024649.5:c.723+164G>A
NG_009093.1:g.14265G>A
NC_000011.10:g.66519912G>A
NC_000011.9:g.66287383G>A
 11/10/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:BBS1
Accession:NM_024649
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001676949 CLINVAR
dbSNP (RS) rs11227515 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene BBS1 CLINVAR
OMIM 209901 CLINVAR