rs36052284 Rat Genome Database

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Variant: rs36052284 -  Homo sapiens

RGD ID: 150472546
RS ID: rs36052284
ClinVar ID: CV1272507
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: MAF  
Reference Nucleotide: -
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 79,628,610
GRCh38 16 79,594,713
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001031804.3:c.*4068dup
NM_005360.5:c.1119-169dup
NG_016440.1:g.11013dup
NC_000016.10:g.79594722dup
More... 		08/15/2019 3 prime utr variant benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV001695563 CLINVAR
dbSNP (RS) rs36052284 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MAF CLINVAR
OMIM 177075 CLINVAR