rs34203493 Rat Genome Database

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Variant: rs34203493 -  Homo sapiens

RGD ID: 150490374
RS ID: rs34203493
ClinVar ID: CV1239104
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EDARADD  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 236,645,346
GRCh38 1 236,482,046
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_145861.4:c.266-221C>T
NG_011566.1:g.92667C>T
NC_000001.11:g.236482046C>T
NC_000001.10:g.236645346C>T
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

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Database
Acc Id
Source(s)
ClinVar RCV001654672 CLINVAR
dbSNP (RS) rs34203493 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene EDARADD CLINVAR
OMIM 606603 CLINVAR