RGD:150513914 Rat Genome Database

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Variant: RGD:150513914 -  Homo sapiens

RGD ID: 150513914
RS ID: rs4843382
ClinVar ID: CV1227963
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 86,543,814
GRCh38 16 86,510,208
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_016273.1:g.4682T>C
NC_000016.10:g.86510208T>C
NC_000016.9:g.86543814T>C
 09/04/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001638241 CLINVAR
dbSNP (RS) rs4843382 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FOXF1 CLINVAR
OMIM 601089 CLINVAR