Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 11:7020491 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and 1 regulatory feature.

Variant displays