Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D
Location

Chromosome 2:208248389 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Missense variant
Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 34 HGVS names - Show

About this variant

This variant overlaps 22 transcripts.

Variant displays