Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/G | Ambiguity code: K
Location

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

Co-located

with dbSNP rs35873857 (T/-)

Most severe consequence
 
Intron variant

This variant has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 25 transcripts.

Variant displays