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 8:19951916 (forward strand) | View in location tab

Co-located

with COSMIC COSM39324 (C/A) ; HGMD-PUBLIC CM900160

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16457

This variation has 5 HGVS names - click the plus to show

Variation displays