Original source

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

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

Chromosome 17:40818165 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays