Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts.

Variant displays