Original source

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

A/G | Ambiguity code: R | MAF: 0.29 (G)

Chromosome 17:15547456 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2505 sample genotypes.

Variant displays