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 2:210298481 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Synonyms

Archive dbSNP rs3197840

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 4 transcripts.

Variant displays