Product Details

SNP ID

rs6826373

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.4:41744443 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACGGTCACGTAGAGGAGACAGTCTG[C/T]ACTGATATTAACACGATACAATTGA

Phenotype

MIM: 603851

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PHOX2B PubMed Links

Gene Details

Gene

PHOX2B

Gene Name

paired like homeobox 2b

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003924.3	2669	UTR 3			NP_003915.2

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