Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D|MAF: 0.13 (A)
Location

Chromosome 2:85625544 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms
HGVS names

This variant has 44 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 32 transcripts and has 4264 sample genotypes.

Variant displays