Original source

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

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

Chromosome 16:88810450 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM900023

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_009_APRT_102600_0005

This variation has 13 HGVS names - click the plus to show

Variation displays