Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.49 (G)
Location

Chromosome 11:128574173 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17807554, rs59799807

This variation has 8 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

Variation displays