Original source

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

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

Chromosome 16:74741806 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs201475928

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and 1 regulatory feature.

Variant displays