Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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