RGD:152031850 Rat Genome Database

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Variant: RGD:152031850 -  Homo sapiens

RGD ID: 152031850
RS ID: rs538845875
ClinVar ID: CV1546155
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNASET2  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 167,352,366
GRCh38 6 166,938,878
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003730.6:c.446+17C>A
NG_016280.2:g.22712C>A
NC_000006.12:g.166938878G>T
NC_000006.11:g.167352366G>T
 12/02/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RNASET2
Accession:NM_003730
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002124645 CLINVAR
dbSNP (RS) rs538845875 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RNASET2 CLINVAR
OMIM 612944 CLINVAR