Original source

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

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

Chromosome 19:33793070 (forward strand) | View in location tab

Co-located

with COSMIC COSM1378 (T/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_017_CEBPA_116897_0003, 807

This variation has 7 HGVS names - click the plus to show

Variation displays