Original source

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

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

Chromosome 11:18393910 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

11:g.18393910C>A

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 23 transcripts.

Variant displays