Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 10:8106006 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM003592

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1730, 2010_April_001_039_GATA3_131320_0005

This variation has 6 HGVS names - click the plus to show

Variation displays