rs1018635371 Rat Genome Database

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Variant: rs1018635371 -  Homo sapiens

RGD ID: 28897172
RS ID: rs1018635371
ClinVar ID: CV863980
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EDARADD  ENO1P1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 236,647,199
GRCh38 1 236,483,899
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.*1250C>T
NG_001115.8:g.902C>T
NG_011566.1:g.94520C>T
NM_145861.2:c.*1250C>T
More... 		01/13/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:EDARADD
Accession:NM_145861
Location:3UTRS;EXON

Gene Symbol:EDARADD
Accession:NM_080738
Location:3UTRS;EXON

Gene Symbol:EDARADD
Accession:NM_001422628
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001102498 CLINVAR
dbSNP (RS) rs1018635371 CLINVAR
MedGen C5848103 CLINVAR
NCBI Gene EDARADD CLINVAR
OMIM 606603 CLINVAR
  614941 CLINVAR