RGD:11661802 Rat Genome Database

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Variant: RGD:11661802 -  Homo sapiens

RGD ID: 11661802
RS ID: rs886048895
ClinVar ID: CV322935
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 106,751,472
GRCh38 12 106,357,694
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_031837.1:g.5037C>A
NC_000012.12:g.106357694C>A
NC_000012.11:g.106751472C>A
NM_018082.5:c.-186C>A
 06/14/2016 2kb upstream variant uncertain significance Pol III-Related Leukodystrophies
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000380182 CLINVAR
dbSNP (RS) rs886048895 CLINVAR
MedGen C5679947 CLINVAR
NCBI Gene POLR3B CLINVAR
OMIM 614366 CLINVAR