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 16:176701 (forward strand) | View in location tab

Co-located

with PhenCode HbVar.1178 (T/C)

Most severe consequence
Evidence status

Synonyms

HbVar 1178

This variation has 3 HGVS names - click the plus to show

Variation displays