Product Details

SNP ID

rs73358041

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:25120213 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGATTTAGTCTCTTCCTGATTTC[A/G]AAGAGCTCATTTACTATTTCGGGAA

Phenotype

MIM: 601491

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

IPW PubMed Links

Gene Details

Gene

IPW

Gene Name

imprinted in Prader-Willi syndrome (non-protein coding)

There are no transcripts associated with this gene.

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