Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.07 (C)
Location

Chromosome 16:3595908 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 5 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Affy GenomeWideSNP_6.0, Illumina_ImmunoChip

About this variant

This variant overlaps 4 transcripts and has 3681 sample genotypes.

Variant displays