RGD:14705699 Rat Genome Database

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Variant: RGD:14705699 -  Homo sapiens

RGD ID: 14705699
RS ID: rs2979687
ClinVar ID: CV663383
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 24,814,403
GRCh38 8 24,956,889
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_008492.1:g.4729A>G
NC_000008.11:g.24956889T>C
NC_000008.10:g.24814403T>C
NM_006158.3:c.-374A>G
More... 		06/19/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000826278 CLINVAR
dbSNP (RS) rs2979687 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NEFL CLINVAR
OMIM 162280 CLINVAR