Product Details

SNP ID: rs9619703
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:21996734 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CATCCCATCACTTTCCACGGTCCAC[A/C]ACAGAGCAGGGCTTTGTGCAAGGAG
Phenotype
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: PRAMENP PubMed Links

Gene Details

There are no transcripts associated with this gene.