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 17:80214672 (forward strand) | View in location tab

Co-located

with COSMIC COSM1189595 (C/T) ; HGMD-PUBLIC CM971361

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_200_SGSH_605270_0005, 13067

This variation has 19 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays