RGD:150517245 Rat Genome Database

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Variant: RGD:150517245 -  Homo sapiens

RGD ID: 150517245
RS ID: rs113827322
ClinVar ID: CV1226693
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 56,225,036
GRCh38 16 56,191,124
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_042800.1:g.4786G>A
NC_000016.10:g.56191124G>A
NC_000016.9:g.56225036G>A
 07/31/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001639787 CLINVAR
dbSNP (RS) rs113827322 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GNAO1 CLINVAR
OMIM 139311 CLINVAR