Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms
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