Product Details

SNP ID: hCV27971267
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:29306700 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGAGAGGGATCTTAAAAAGATTGT[G/A]TTTCAATTATTGGTTAATTCCTTTC
Phenotype
Polymorphism: G/A, Transition substitution
Allele Nomenclature
Literature Links: SNX29P2 PubMed Links

Gene Details

There are no transcripts associated with this gene.