Product Details
- SNP ID
-
rs2625529
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:71826436 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- CTTCTGCAGGAGGCCCAGGAATTCA[C/G]CACATACAGTCTTAGCCATATGCTT
- Phenotype
-
MIM: 604875
MIM: 604485
- Polymorphism
- C/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
MYO9A
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs55764190] 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
- MYO9A
- Gene Name
- myosin IXA
- Gene
- NR2E3
- Gene Name
- nuclear receptor subfamily 2 group E member 3
There are no transcripts associated with this gene.
View Full Product Details