Original source

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

Alleles
A/C/T|Ancestral: T|Ambiguity code: H|MAF: 0.18 (A)
Location

Chromosome 6:1613294 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays