Product Details

SNP ID

rs11126180

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:68136779 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTATTGGTCTAACGCCATAATACC[A/G]CATTTCCCTCTCAGCTACCTCAAAT

Phenotype

MIM: 610729

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

WDR92 PubMed Links

Gene Details

Gene

WDR92

Gene Name

WD repeat domain 92

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256476.1		Intron			NP_001243405.1
NM_138458.3		Intron			NP_612467.1

View Full Product Details