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 11:72242428 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 3 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 1 sample genotype.

Variant displays