RGD:150493911 Rat Genome Database

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Variant: RGD:150493911 -  Homo sapiens

RGD ID: 150493911
RS ID: rs10120023
ClinVar ID: CV1257652
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 137,810,259
GRCh38 9 134,918,413
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_046982.2:g.4548G>A
NC_000009.12:g.134918413C>T
NC_000009.11:g.137810259C>T
 08/22/2019 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001675325 CLINVAR
dbSNP (RS) rs10120023 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FCN1 CLINVAR
OMIM 601252 CLINVAR