Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.40 (A)

Chromosome 11:47447017 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57455549

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3674 sample genotypes and is associated with 2 phenotypes.

Variant displays