Product Details

SNP ID

rs8097360

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:2853872 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGACATTTCTTACAGCCTCCAATAC[C/G]CATTGGTAGTGTTTGGACGTACGGC

Phenotype

MIM: 608928

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

EMILIN2 PubMed Links

Additional Information

For this assay, SNP(s) [rs114349868] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

EMILIN2

Gene Name

elastin microfibril interfacer 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032048.2		Intron			NP_114437.2
XM_017026038.1		Intron			XP_016881527.1

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