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 6:10404509 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM102900, CM085950

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_003220.2:c.763A>G, 444

This variation has 23 HGVS names - click the plus to show

Variation displays