Product Details
- SNP ID
-
rs7754862
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:157716941 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TCAGTGTCCAGTACCTCTGTCCTTT[C/G]CGAACCCCTGCTCAGCAATCCCATG
- Phenotype
-
MIM: 605952
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
SNX9
PubMed Links
Gene Details
- Gene
- SNX9
- Gene Name
- sorting nexin 9
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