Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W
Location

Chromosome 11:17075592 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 14 transcripts.

Variant displays