Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)

Chromosome 20:958880 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs52825576

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts and has 3523 sample genotypes.

Variant displays