Original source

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

G/A | Ambiguity code: R | MAF: 0.14 (A)

Chromosome 10:133533455 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60190482

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3757 sample genotypes and is mentioned in 4 citations.

Variant displays