RGD:150455957 Rat Genome Database

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Variant: RGD:150455957 -  Homo sapiens

RGD ID: 150455957
RS ID: rs1952013
ClinVar ID: CV1249543
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 14 50,087,357
GRCh38 14 49,620,639
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_008920.1:g.4869C>G
NG_033054.1:g.4993G>C
NC_000014.9:g.49620639C>G
NC_000014.8:g.50087357C>G
 06/29/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001668758 CLINVAR
dbSNP (RS) rs1952013 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MGAT2 CLINVAR
OMIM 602616 CLINVAR