RGD:150495607 Rat Genome Database

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Variant: RGD:150495607 -  Homo sapiens

RGD ID: 150495607
RS ID: rs72982956
ClinVar ID: CV1272674
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 73,661,251
GRCh38 11 73,950,206
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_053111.1:g.4888G>A
NC_000011.10:g.73950206G>A
NC_000011.9:g.73661251G>A
 12/17/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001688597 CLINVAR
dbSNP (RS) rs72982956 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNAJB13 CLINVAR
OMIM 610263 CLINVAR