Product Details

SNP ID: rs2836655
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.21:38744120 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GCAAAAAGATCCGTCTTTTCCCCAC[C/T]ACGGTAAAAAAAAACGTAATTCCTT
Phenotype: MIM: 611723
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: LINC00114 PubMed Links
Additional Information: For this assay, SNP(s) [rs145111784] 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

There are no transcripts associated with this gene.