Original source

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

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

Chromosome 2:54971937 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and is mentioned in 1 citation.

Variant displays