Product Details
- SNP ID
-
rs6966470
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:123659801 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GAATGCGTCTGAGGGATATTTGGAG[A/G]GGATGTCAAAGAAGGCTTTCTGGGA
- Phenotype
-
MIM: 608006
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
LMOD2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs28705875] 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
- LMOD2
- Gene Name
- leiomodin 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_207163.1 |
|
Intron |
|
|
NP_997046.1 |
View Full Product Details