RGD:150466301 Rat Genome Database

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Variant: RGD:150466301 -  Homo sapiens

RGD ID: 150466301
RS ID: rs3733742
ClinVar ID: CV1268750
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 68,788,261
GRCh38 5 69,492,434
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_028291.1:g.5143G>A
NC_000005.10:g.69492434G>A
NC_000005.9:g.68788261G>A
 09/17/2019 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001694447 CLINVAR
dbSNP (RS) rs3733742 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene OCLN CLINVAR
OMIM 602876 CLINVAR