Original source

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

Alleles
C/A/G | Ancestral: C | Ambiguity code: V
Location

Chromosome 16:177040 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940889

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

Variation displays