Original source

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

A/G/T | Ancestral: G | Ambiguity code: D | MAF: 0.41 (A)

Chromosome 17:18365454 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 2510 sample genotypes.

Variant displays