Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs3743783

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 14 transcripts, has 2775 sample genotypes and is mentioned in 2 citations.

Variant displays