Original source

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

Alleles
A/T|Ambiguity code: W
Location

Chromosome 17:43100655 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 27 HGVS names - Show

About this variant

This variant overlaps 27 transcripts.

Variant displays