Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variants

COSMIC COSM41680, COSM1561233 ; HGMD-PUBLIC CM011940

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 1733, 2010_April_001_041_GATA3_131320_0008

HGVS names

This variant has 6 HGVS names - Show

About this variant

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

Variant displays