Original source

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

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

Chromosome 3:16586835 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts.

Variant displays