Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (C)

Chromosome 16:1509964 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs56689278

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2507 sample genotypes.

Variant displays