rs7540171 Rat Genome Database

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Variant: rs7540171 -  Homo sapiens

RGD ID: 150444206
RS ID: rs7540171
ClinVar ID: CV1249383
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MACF1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 39,920,378
GRCh38 1 39,454,706
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001394062.1:c.20887-203A>G
NG_050926.1:g.378290A>G
NC_000001.11:g.39454706A>G
NC_000001.10:g.39920378A>G
More... 		05/13/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MACF1
Accession:NM_001397473
Location:INTRON

Gene Symbol:MACF1
Accession:NM_012090
Location:INTRON

Gene Symbol:MACF1
Accession:NM_001394062
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001666815 CLINVAR
dbSNP (RS) rs7540171 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MACF1 CLINVAR
OMIM 608271 CLINVAR