Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.19 (G)
Location

Chromosome 5:14186599 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386143, rs61109634, rs1302354

HGVS names

This variant has 6 HGVS names - Show

About this variant

Variant displays