rs72797524 Rat Genome Database

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Variant: rs72797524 -  Homo sapiens

RGD ID: 14723657
RS ID: rs72797524
ClinVar ID: CV665110
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNA2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 70,231,304
GRCh38 10 68,471,547
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001080449.3:c.74+244C>T
NG_034247.1:g.5427C>T
NG_046972.1:g.60977C>T
NC_000010.11:g.68471547G>A
More... 		06/16/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DNA2
Accession:XM_006717680
Location:INTRON

Gene Symbol:DNA2
Accession:XM_011539417
Location:INTRON

Gene Symbol:DNA2
Accession:NM_001080449
Location:INTRON

Gene Symbol:DNA2
Accession:XM_017015799
Location:INTRON

Gene Symbol:DNA2
Accession:NR_102264
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000832638 CLINVAR
dbSNP (RS) rs72797524 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNA2 CLINVAR
OMIM 601810 CLINVAR