RGD:14717913 Rat Genome Database

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Variant: RGD:14717913 -  Homo sapiens

RGD ID: 14717913
RS ID: rs12002679
ClinVar ID: CV663803
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 137,533,634
GRCh38 9 134,641,788
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000009.11:g.137533634C>G
NM_000093.3:c.-400C>G
NG_008030.1:g.4983C>G
NC_000009.12:g.134641788C>G
More... 		06/18/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000830220 CLINVAR
dbSNP (RS) rs12002679 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL5A1 CLINVAR
OMIM 120215 CLINVAR