Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.01 (A)
Location

Chromosome 11:116790676 (forward strand) | View in location tab

Co-located

with COSMIC COSM686256 (C/T) ; HGMD-PUBLIC CM032546

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

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

Variation displays