Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 10:8073747 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM065214

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_042_GATA3_131320_0012, 1737

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

Variation displays