RGD:150331450 Rat Genome Database

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Variant: RGD:150331450 -  Homo sapiens

RGD ID: 150331450
RS ID: rs9912067
ClinVar ID: CV1169737
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130061159  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 17 48,423,418
GRCh38 17 50,346,057
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_012175.1:g.5026G>A
NC_000017.11:g.50346057G>A
NC_000017.10:g.48423418G>A
 05/19/2021 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001536480 CLINVAR
dbSNP (RS) rs9912067 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC130061159 CLINVAR
  XYLT2 CLINVAR
OMIM 608125 CLINVAR