Product Details
- SNP ID
-
rs10496572
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:121759938 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- AGATAAGAATATGTAACAGTGAAAG[C/T]GTCCCACAAAGCCTAAAATATTTAC
- Phenotype
-
MIM: 600575
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TSN
PubMed Links
Gene Details
- Gene
- TSN
- Gene Name
- translin
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