Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.32 (C)
Location

Chromosome 16:86369512 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61494603

HGVS name

16:g.86369512C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_Human660W-quad, Illumina_ImmunoChip

Variation displays