Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 12:52789244 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58116199

HGVS name

12:g.52789244C>T

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Affy GeneChip 500K, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 3339 sample genotypes.

Variant displays