Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and 1 regulatory feature.

Variant displays