Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.11 (C)
Location

Chromosome 16:88809263 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs117716417, rs8191506

HGVS name

16:g.88809263T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays