Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.23 (T)
Location

Chromosome 11:27658369 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020369

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 44 HGVS names - click the plus to show

This variation has assays on 15 chips - click the plus to show

Variation displays