Product Details

SNP ID: hCV166463826
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.1:146018454 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCTGAGAAGGCCATGGCCACATCCT[T/C]TGCTACCTTGATGGAGAAGGAGAGC
Phenotype: MIM: 608374
Polymorphism: T/C, Transition substitution
Allele Nomenclature
Literature Links: HFE2 PubMed Links

Gene Details

There are no transcripts associated with this gene.