Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 8 HGVS names - click the plus to show

About this variant

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

Variant displays