rs30412 Rat Genome Database

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Variant: rs30412 -  Homo sapiens

RGD ID: 150447663
RS ID: rs30412
ClinVar ID: CV1270343
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAF  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 79,628,172
GRCh38 16 79,594,275
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005360.5:c.*185G>C
NM_001031804.3:c.*4506G>C
NG_016440.1:g.11451G>C
NC_000016.10:g.79594275C>G
More... 		06/26/2018 3 prime utr variant benign none provided

Gene Symbol:MAF
Accession:NM_005360
Location:3UTRS;EXON

Gene Symbol:MAF
Accession:NM_001031804
Location:3UTRS;EXON

Gene Symbol:MAF
Accession:XM_017023234
Location:INTRON

Gene Symbol:MAF
Accession:XM_017023235
Location:INTRON

Gene Symbol:MAF
Accession:XM_017023233
Location:INTRON

Gene Symbol:MAF
Accession:XM_024450279
Location:INTRON

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

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

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

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

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001691480 CLINVAR
dbSNP (RS) rs30412 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MAF CLINVAR
OMIM 177075 CLINVAR