Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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 COSM41680 (C/T), COSM1561233 (C/A) ; 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

About this variant

This variant overlaps 3 transcripts and is associated with 2 phenotypes.

Variation displays