Original source

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

G/A | Ambiguity code: R | MAF: 0.31 (G)

Chromosome 10:133536033 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59502658

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 9 transcripts and has 3858 sample genotypes.

Variant displays