Original source

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

Alleles
G/T|Ancestral: T|Ambiguity code: K|MAF: 0.36 (G)
Location

Chromosome 4:88028023 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59969938, rs17786390

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

Variant displays