Original source

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

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

Chromosome 17:40818348 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant

This variant has 2 HGVS names - click the plus to show

About this variant

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

Variant displays