Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.10 (A)

Chromosome 10:49625793 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59127410

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 7 transcripts, has 3794 sample genotypes and is mentioned in 3 citations.

Variant displays