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: 0.01 (T)
Location

Chromosome 11:114058254 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.114058254C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays