Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K
Location

Chromosome 11:18394493 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 23 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays