Product Details
- SNP ID
-
rs62639328
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:45795907 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCCTCGCCCTCCTCCTCCTCCTCGC[C/T]CTCCTCCTCCTCCTCTGTGGCTCCC
- Phenotype
-
MIM: 609857
MIM: 607548
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
DMWD
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs557359374] 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
- Gene
- DMWD
- Gene Name
- dystrophia myotonica, WD repeat containing
There are no transcripts associated with this gene.
- Gene
- RSPH6A
- Gene Name
- radial spoke head 6 homolog A
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