Product Details
- SNP ID
-
rs6996272
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:2046092 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CACTTGTGGCACAGGCCAACGCTGC[G/T]TGTCTGGGAGTCCCTTTCCCCTCTA
- Phenotype
-
MIM: 603509
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
MYOM2
PubMed Links
Gene Details
- Gene
- MYOM2
- Gene Name
- myomesin 2
View Full Product Details