Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.37 (A)
Location

Chromosome 11:3802299 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60161749

HGVS names

This variant has 20 HGVS names - Show

About this variant

Variant displays