Original source

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

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

Chromosome 16:176752 (forward strand) | View in location tab

Co-located

with dbSNP rs33996902 (C/G/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB HbVar.14_1, HbVar.14_3

This variation has 12 HGVS names - click the plus to show

Variation displays