Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.24 (G)
Location

Chromosome 16:50741834 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3743783

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 15 transcripts, has 2775 individual genotypes and is mentioned in 2 citations.

Variation displays