Original source

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

Alleles
T/G|Ambiguity code: K
Location

Chromosome 11:18402472 (forward strand)|View in location tab

Co-located variant

dbSNP rs35873857 (T/-)

Most severe consequence
 
Intron variant
HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 25 transcripts.

Variant displays