Original source

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

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

Chromosome 14:73170945 (forward strand) | View in location tab


with HGMD-PUBLIC CM981649

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 35 HGVS names - click the plus to show

Variation displays