Original source

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

Alleles
A/G/T | Ancestral: A | Ambiguity code: D
Location

Chromosome 4:73413589 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM995269, CM973674

Most severe consequence
Evidence status

Synonyms

LSDB Bergamo, Brest

This variation has 38 HGVS names - click the plus to show

Variation displays