Original source

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

G/A | Ambiguity code: R | MAF: 0.30 (A)

Chromosome 22:36281354 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs57513093, rs7525, rs3197056

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 3 transcripts and has 3685 sample genotypes.

Variant displays