Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.21 (A)

Chromosome 14:23118022 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57051532

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3046 sample genotypes and is associated with 1 phenotype.

Variant displays