Original source

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

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

Chromosome 11:102777459 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts.

Variant displays