Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.22 (C)
Location

Chromosome 16:50803756 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 13 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni1-Quad, Illumina_ImmunoChip

Variation displays