RGD:150415573 Rat Genome Database

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Variant: RGD:150415573 -  Homo sapiens

RGD ID: 150415573
RS ID: rs55940468
ClinVar ID: CV1192318
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 21 46,131,756
GRCh38 21 44,711,841
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_033806.1:g.4740A>G
NC_000021.9:g.44711841T>C
NC_000021.8:g.46131756T>C
 02/14/2019 likely benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001568046 CLINVAR
dbSNP (RS) rs55940468 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TSPEAR CLINVAR
OMIM 612920 CLINVAR