rs41278962 Rat Genome Database

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Variant: rs41278962 -  Homo sapiens

RGD ID: 150466048
RS ID: rs41278962
ClinVar ID: CV1268709
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PARK7  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 8,029,319
GRCh38 1 7,969,259
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001123377.2:c.193-86A>G
NM_007262.5:c.193-86A>G
NG_008271.1:g.12606A>G
NC_000001.11:g.7969259A>G
More... 		09/04/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PARK7
Accession:NM_007262
Location:INTRON

Gene Symbol:PARK7
Accession:NM_001123377
Location:INTRON

Gene Symbol:PARK7
Accession:XM_005263424
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001694405 CLINVAR
dbSNP (RS) rs41278962 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PARK7 CLINVAR
OMIM 602533 CLINVAR