Product Details
- SNP ID
-
rs1999506
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
64
- Location
-
Chr.1:236399987 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CAACCTACCCTCCTGTGGCATTGGG[C/T]GCAGTACCCAGGACTAAAGGATAAA
- Phenotype
-
MIM: 606603
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
EDARADD
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs147443884] are located under a probe and SNP(s) [rs188761780] are located under a primer 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
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