Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.01 (C)

Chromosome 11:27659648 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status


Archive dbSNP rs28405820, rs11602143

HGVS names

This variant has 27 HGVS names - Show

About this variant

This variant overlaps 27 transcripts and has 2504 sample genotypes.

Variant displays