Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 17:44851109 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM040820

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_239_WNT3_165330_0001, 4495

This variation has 3 HGVS names - click the plus to show

17:g.44851109G>A
ENST00000225512.5:c.247C>T
ENSP00000225512.5:p.Gln83Ter

Variation displays