Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 7 citations.

Variant displays