Original source

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

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

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

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

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