RGD:28892059 Rat Genome Database

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Variant: RGD:28892059 -  Homo sapiens

RGD ID: 28892059
RS ID: rs765434534
ClinVar ID: CV886038
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GSS  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 33,516,611
GRCh38 20 34,928,808
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001322495.1:c.*20G>C
LRG_1168:g.32220G>C
NM_000178.2:c.*20G>C
NG_008848.2:g.32220G>C
More... 		01/13/2018 3 prime utr variant likely benign|uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:GSS
Accession:NM_001322494
Location:3UTRS;EXON

Gene Symbol:GSS
Accession:NM_001322495
Location:3UTRS;EXON

Gene Symbol:GSS
Accession:NM_000178
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001139606 CLINVAR
  RCV001564782 CLINVAR
dbSNP (RS) rs765434534 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GSS CLINVAR
OMIM 601002 CLINVAR