Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 11:112026270 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 8 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 7 transcripts and has 32 sample genotypes.

Variant displays