Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.03 (A)
Location

Chromosome 11:17074911 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

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

Variation displays