RGD:150496069 Rat Genome Database

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Variant: RGD:150496069 -  Homo sapiens

RGD ID: 150496069
RS ID: rs537395792
ClinVar ID: CV1272790
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 56,225,131
GRCh38 16 56,191,219
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_042800.1:g.4881G>T
NC_000016.10:g.56191219G>T
NC_000016.9:g.56225131G>T
 07/26/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001688713 CLINVAR
dbSNP (RS) rs537395792 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GNAO1 CLINVAR
OMIM 139311 CLINVAR