Product Details
- SNP ID
-
rs10799551
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
70
- Location
-
Chr.1:224239469 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- CTATGGTGGTGGGGCTGCCACATTA[T/G]GTAGGAGCCCTTGTTAGGTGCTTTC
- Phenotype
-
MIM: 602426
- Polymorphism
- T/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
NVL
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs76962725] 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
- NVL
- Gene Name
- nuclear VCP-like
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