RGD:14708539 Rat Genome Database

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Variant: RGD:14708539 -  Homo sapiens

RGD ID: 14708539
RS ID: rs761193810
ClinVar ID: CV670234
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GSS  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 33,519,738
GRCh38 20 34,931,935
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000020.10:g.33519738G>A
NM_000178.2:c.1029+4C>T
NM_000178.4:c.1029+4C>T
NM_001322494.1:c.1029+4C>T
More... 		05/30/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GSS
Accession:NM_001322494
Location:INTRON

Gene Symbol:GSS
Accession:NM_000178
Location:INTRON

Gene Symbol:GSS
Accession:NM_001322495
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000827181 CLINVAR
dbSNP (RS) rs761193810 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene GSS CLINVAR
OMIM 601002 CLINVAR