Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.01 (G)
Location

Chromosome 11:112087953 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM022244

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 21 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

Variation displays