Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K
Location

Chromosome 17:43121305 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 25 HGVS names - Show

About this variant

This variant overlaps 27 transcripts.

Variant displays