rs635487 Rat Genome Database

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Variant: rs635487 -  Homo sapiens

RGD ID: 150511256
RS ID: rs635487
ClinVar ID: CV1212685
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EDARADD  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 236,590,816
GRCh38 1 236,427,516
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_145861.4:c.219+66T>G
NG_011566.1:g.38137T>G
NC_000001.11:g.236427516T>G
NC_000001.10:g.236590816T>G
More... 		11/11/2018 intron variant benign none provided

Gene Symbol:EDARADD
Accession:NM_145861
Location:INTRON

Gene Symbol:EDARADD
Accession:NM_080738
Location:INTRON

Gene Symbol:EDARADD
Accession:NM_001422628
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001597916 CLINVAR
dbSNP (RS) rs635487 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene EDARADD CLINVAR
OMIM 606603 CLINVAR