Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 16:47665993 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Synonyms

Archive dbSNP rs3190593

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 1 sample genotype.

Variant displays