Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.05 (T)
Location

Chromosome 11:120234838 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.120234838C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5, Illumina_Human1M-duo

Variation displays