Original source

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

A/C | Ancestral: A | Ambiguity code: M

Chromosome 2:9628734 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and 1 regulatory feature.

Variant displays