Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.37 (C)
Location

Chromosome 11:2328948 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3782054

This variation has 16 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5

Variation displays