Original source

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

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

Chromosome 17:40818348 (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