Original source

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

G/T | Ancestral: T | Ambiguity code: K | MAF: 0.16 (G)

Chromosome 22:36812105 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs52816418, rs57904463

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 7 transcripts, has 2878 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays