Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.34 (C)
Location

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

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs61494603

HGVS name

16:g.86369512C>T

Genotyping chips

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

About this variant

This variant has 3050 sample genotypes, is associated with 1 phenotype and is mentioned in 6 citations.

Variant displays