Product Details
- SNP ID
-
rs6088445
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.20:31516023 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTCCCCAGGAGCAGAGAACTCACTA[C/T]TGGCTCTGTATGCGATCAGATGCAA
- Phenotype
-
MIM: 607106
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
HM13
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs75035893] 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
- HM13
- Gene Name
- histocompatibility minor 13
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