Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.06 (G)
Location

Chromosome 16:28879222 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 6 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

Variant displays