Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.18 (A)
Location

Chromosome 11:6394233 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

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

Variation displays