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 17:80210856 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981805, CM002400

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_202_SGSH_605270_0009, 13071

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

Variation displays