Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 17:28726312 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 24 transcripts and 1 regulatory feature.

Variant displays