Product Details
- SNP ID
-
rs4929922
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:8954229 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CAGAAAGTAGACTAGTGACCGAGTA[A/G]GGCTGGAAATGGGAATTAACTGTAA
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TMEM9B
PubMed Links
Gene Details
- Gene
- TMEM9B
- Gene Name
- TMEM9 domain family member B
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