Product Details

SNP ID
rs592627
Assay Type
Functionally Tested
NCBI dbSNP Submissions
68
Location
Chr.1:236404138 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCCCGCTTCTCCTCTGCTCCTCTGC[A/C]CGTCCTATTAGATATCAGAGCCTTG
Phenotype
MIM: 606603
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
EDARADD PubMed Links
Additional Information
For this assay, SNP(s) [rs75148280] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
EDARADD
Gene Name
EDAR associated death domain
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_080738.3 Intron NP_542776.1
NM_145861.2 Intron NP_665860.2

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