Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.02 (G)
Location

Chromosome 16:88811521 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

About this variant

Variant displays