Original source

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

G/C|Ancestral: C|Ambiguity code: S|MAF: 0.21 (G)

Chromosome 11:22193357 (forward strand)|View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

Clinical significance

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 2511 sample genotypes and is associated with 1 phenotype.

Variant displays