rs1759388 Rat Genome Database

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Variant: rs1759388 -  Homo sapiens

RGD ID: 150472221
RS ID: rs1759388
ClinVar ID: CV1217145
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EDARADD  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 236,590,497
GRCh38 1 236,427,197
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_145861.4:c.161-195C>G
NG_011566.1:g.37818C>G
NC_000001.11:g.236427197C>G
NC_000001.10:g.236590497C>G
More... 		11/11/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:EDARADD
Accession:NM_145861
Location:INTRON

Gene Symbol:EDARADD
Accession:NM_080738
Location:INTRON

Gene Symbol:EDARADD
Accession:NM_001422628
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001615440 CLINVAR
dbSNP (RS) rs1759388 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene EDARADD CLINVAR
OMIM 606603 CLINVAR