Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.25 (C)

Chromosome 16:50769845 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 10 transcripts, has 3974 sample genotypes and is mentioned in 1 citation.

Variant displays