Original source

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

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

Chromosome 11:112045279 (forward strand) | View in location tab

Co-located

with dbSNP rs373885044 (G/-)

Most severe consequence
 
Intron variant

This variant has 5 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and 1 regulatory feature.

Variant displays