Original source

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

Alleles
T/G|Ambiguity code: K
Location

Chromosome 8:45589154 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript.

Variant displays