RGD:150449968 Rat Genome Database

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Variant: RGD:150449968 -  Homo sapiens

RGD ID: 150449968
RS ID: rs140412529
ClinVar ID: CV1232618
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 57,993,921
GRCh38 3 58,008,194
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_012801.1:g.4795C>T
NC_000003.12:g.58008194C>T
NC_000003.11:g.57993921C>T
 06/30/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001647693 CLINVAR
dbSNP (RS) rs140412529 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FLNB CLINVAR
OMIM 603381 CLINVAR