Product Details
- SNP ID
-
rs6758117
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:176082509 on Build GRCh38
- Set Membership
-
Validated
- Context Sequence [VIC/FAM]
- TGTAGGACCAACAGCCCGGCGCTGG[C/T]GCTGCGCGCGGATCGGGGAAGCCCC
- Phenotype
-
MIM: 142991
MIM: 142989
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
EVX2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs72919090] 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
- EVX2
- Gene Name
- even-skipped homeobox 2
- Gene
- HOXD13
- Gene Name
- homeobox D13
There are no transcripts associated with this gene.
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