Original source

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

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

Chromosome 10:8073787 (forward strand) | View in location tab

Co-located

with COSMIC COSM1561233 (C/A), COSM41680 (C/T) ; HGMD-PUBLIC CM011940

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1733, 2010_April_001_041_GATA3_131320_0008

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

Variation displays