This variant has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_239_WNT3_165330_0001, 4495

HGVS name

None

About this variant

This variant is associated with 6 phenotypes.

Variant displays