rs4081752 Rat Genome Database

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Variant: rs4081752 -  Homo sapiens

RGD ID: 150463841
RS ID: rs4081752
ClinVar ID: CV1206789
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAF  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 79,633,887
GRCh38 16 79,599,990
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000016.9:g.79633887G>A
NM_001031804.3:c.-88C>T
NM_005360.5:c.-88C>T
NG_016440.1:g.5736C>T
More... 		09/22/2018 5 prime utr variant likely benign none provided

Gene Symbol:MAF
Accession:NM_005360
Location:5UTRS;EXON

Gene Symbol:MAF
Accession:NM_001031804
Location:5UTRS;EXON

Gene Symbol:MAF
Accession:XM_017023234
Location:5UTRS;EXON

Gene Symbol:MAF
Accession:XM_017023235
Location:5UTRS;EXON

Gene Symbol:MAF
Accession:XM_017023233
Location:5UTRS;EXON

Gene Symbol:MAF
Accession:XM_024450279
Location:5UTRS;EXON

Gene Symbol:MAF
Accession:XR_001751902
Location:EXON;NON-CODING

Gene Symbol:MAF
Accession:XR_002957804
Location:EXON;NON-CODING

Gene Symbol:MAF
Accession:XR_002957803
Location:EXON;NON-CODING

Gene Symbol:MAF
Accession:XR_002957802
Location:EXON;NON-CODING

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001587190 CLINVAR
dbSNP (RS) rs4081752 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MAF CLINVAR
OMIM 177075 CLINVAR