Original source

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

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

Chromosome 17:63488364 (forward strand) | View in location tab

Most severe consequence
Intron variant

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays