rs2021976 Rat Genome Database

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Variant: rs2021976 -  Homo sapiens

RGD ID: 150491873
RS ID: rs2021976
ClinVar ID: CV1280682
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SURF1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 136,218,889
GRCh38 9 133,352,034
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001280787.1:c.506+27C>T
NM_003172.4:c.833+27C>T
NG_008477.1:g.9473C>T
NC_000009.12:g.133352034G>A
More... 		06/29/2018 intron variant benign none provided

Gene Symbol:SURF1
Accession:NM_001280787
Location:INTRON

Gene Symbol:SURF1
Accession:NM_003172
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001716713 CLINVAR
dbSNP (RS) rs2021976 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SURF1 CLINVAR
OMIM 185620 CLINVAR