Original source

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

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

Chromosome 16:86403118 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61494603

HGVS name

16:g.86403118C>T

Genotyping chips

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

Variation displays