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 17:82078483 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 5 transcripts and has 248 sample genotypes.

Variant displays