Product Details

SNP ID

rs2083797

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:46844563 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAAATGGTGTGGTGGTGGCCGATT[C/T]CTAAAACTAACTGCAAAGGATTGCA

Phenotype

MIM: 602864

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WNT9B PubMed Links

Gene Details

Gene

WNT9B

Gene Name

Wnt family member 9B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320458.1		Intron			NP_001307387.1
NM_003396.2		Intron			NP_003387.1
XM_011525178.2		Intron			XP_011523480.1

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