RGD:14705831 Rat Genome Database

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Variant: RGD:14705831 -  Homo sapiens

RGD ID: 14705831
RS ID: rs11122043
ClinVar ID: CV658050
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC120851202  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 6,580,429
GRCh38 1 6,520,369
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000001.11:g.6520369C>T
NM_020631.4:c.-28820G>A
NG_073742.1:g.181C>T
NC_000001.10:g.6580429C>T
More... 		06/18/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000826323 CLINVAR
dbSNP (RS) rs11122043 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC120851202 CLINVAR
  PLEKHG5 CLINVAR
OMIM 611101 CLINVAR