Product Details

SNP ID: rs12766020
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:97001652 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AGAGGCTGGAGGCCCCGGGGGCAAT[A/G]ACATTATGAAAAGGATTCATGCTGG
Phenotype: MIM: 603742
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: SLIT1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003061.2		Intron			NP_003052.2