RGD:150443159 Rat Genome Database

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Variant: RGD:150443159 -  Homo sapiens

RGD ID: 150443159
RS ID: rs6547675
ClinVar ID: CV1287843
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 86,565,371
GRCh38 2 86,338,248
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_713:g.4836T>C
NG_013037.1:g.4836T>C
NC_000002.12:g.86338248A>G
NC_000002.11:g.86565371A>G
 07/08/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001725564 CLINVAR
dbSNP (RS) rs6547675 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene REEP1 CLINVAR
OMIM 609139 CLINVAR