Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 3 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

Variant displays