Product Details

SNP ID

rs11926637

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:13822041 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGAAAGGCAAATCAAAACCACAAC[A/G]ACATGCTCCTTTACACTCACTAGGA

Phenotype

MIM: 601570

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

WNT7A PubMed Links

Gene Details

Gene

WNT7A

Gene Name

Wnt family member 7A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004625.3		Intron			NP_004616.2
XM_011534091.2		Intron			XP_011532393.1

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