Product Details

SNP ID
rs217127
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:108221496 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AATCTTCAACAGTAAACATTCCAAA[C/T]GAGGAATACAGTATTACAAGGAATA
Phenotype
MIM: 605930
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SNX3 PubMed Links

Gene Details

Gene
SNX3
Gene Name
sorting nexin 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001300928.1 Intron NP_001287857.1
NM_001300929.1 Intron NP_001287858.1
NM_003795.5 Intron NP_003786.1
NM_152827.3 Intron NP_690040.1

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