Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D
Location

Chromosome 16:3596232 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs3169472

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2 sample genotypes.

Variant displays