Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 8:90970988 (forward strand) | View in location tab

Co-located

with COSMIC COSM245943 (G/A) ; HGMD-PUBLIC CM054792

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11344

This variation has 15 HGVS names - click the plus to show

Variation displays