Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 21:25891793 (forward strand) | View in location tab

Co-located

with COSMIC COSM1029634 (T/C) ; HGMD-PUBLIC CM021245

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 18 HGVS names - click the plus to show

Variation displays