Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.46 (G)
Location

Chromosome 11:118959331 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60012314, rs56459440

This variation has 46 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays