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 17:39688086 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 18 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays