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SNP ID

rs13195185

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:160217964 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAATTGCAAGTTTTCTCAATCATC[G/T]TGTCTTCGTGAATGCCAGGACATTG

Phenotype

MIM: 602608

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

SLC22A2 PubMed Links

Gene Details

Gene

SLC22A2

Gene Name

solute carrier family 22 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003058.3		Intron			NP_003049.2

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