Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 17:63918016 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS951426, CS951425, CS075157

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB GH1_291+1G_C_040511

This variation has 16 HGVS names - click the plus to show

Variation displays