Original source

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

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

Chromosome 9:27548425 (forward strand)|View in location tab

Most severe consequence
 
Splice region variant
HGVS names

This variant has 4 HGVS names - Show

About this variant

Variant displays