Original source

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

A/G/T|Ancestral: A|Ambiguity code: D|MAF: 0.06 (G)

Chromosome 12:122769991 (forward strand)|View in location tab

Co-located variant

dbSNP rs545336826 (A/G)

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 14 transcripts and has 3007 sample genotypes.

Variant displays