Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.33 (A)

Chromosome 11:120236702 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs60085109

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 6 transcripts and has 3881 sample genotypes.

Variant displays