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 16:23380731 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM056053, CM050080, CM951144

Most severe consequence
Synonyms

LSDB 9509, 9503

This variation has 20 HGVS names - click the plus to show

Variation displays