RGD:150494585 Rat Genome Database

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Variant: RGD:150494585 -  Homo sapiens

RGD ID: 150494585
RS ID: rs7656433
ClinVar ID: CV1256488
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FGA  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 155,510,224
GRCh38 4 154,589,072
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000508.5:c.181-96T>A
NM_021871.4:c.181-96T>A
LRG_557:g.6674T>A
NG_008832.1:g.6674T>A
More... 		11/11/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FGA
Accession:NM_021871
Location:INTRON

Gene Symbol:FGA
Accession:NM_000508
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001675453 CLINVAR
dbSNP (RS) rs7656433 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FGA CLINVAR
OMIM 134820 CLINVAR