Product Details

SNP ID

rs11190568

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:100464520 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGATTCCCTTCCCTAGTCACCAGGG[C/T]GGTGTGAAGAATTGTTCTATAAAAA

Phenotype

MIM: 601396

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WNT8B PubMed Links

Gene Details

Gene

WNT8B

Gene Name

Wnt family member 8B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003393.3		Intron			NP_003384.2

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