Product Details

SNP ID

rs8113792

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:2294261 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TACAGGGGAAATAGAGCCGTGTGAA[C/G]ACGGAGGCAGAGGCTAGGGTGACAC

Phenotype

MIM: 609792

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

LINGO3 PubMed Links

Gene Details

Gene

LINGO3

Gene Name

leucine rich repeat and Ig domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001101391.1		Intron			NP_001094861.1

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