Product Details

SNP ID: rs937662
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:38678593 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GCGAGAGAACAGAGTTTTGCTCTTG[C/T]TCCTCCCTCACTGCTGTGTGCATCG
Phenotype: MIM: 138750
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: GLO1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006708.2		Intron			NP_006699.2