RGD:14723322 Rat Genome Database

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Variant: RGD:14723322 -  Homo sapiens

RGD ID: 14723322
RS ID: rs1800732
ClinVar ID: CV665134
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 6,640,753
GRCh38 11 6,619,522
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_033858.2:g.41328T>C
NG_008653.1:g.4940T>C
NC_000011.10:g.6619522A>G
NC_000011.9:g.6640753A>G
More... 		06/19/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000832481 CLINVAR
dbSNP (RS) rs1800732 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TPP1 CLINVAR
OMIM 607998 CLINVAR