Product Details
- SNP ID
-
rs141218257
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:68343859 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCAAGTCAGTCAGTGTTGATACATG[A/G]GTTTTGAAAAGTGAGAAACTTACTT
- Phenotype
-
MIM: 602324
MIM: 610328
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
HNRNPH3
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs146249363] 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
- HNRNPH3
- Gene Name
- heterogeneous nuclear ribonucleoprotein H3
- Gene
- RUFY2
- Gene Name
- RUN and FYVE domain containing 2
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