Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.22 (A)
Location

Chromosome 14:20472447 (forward strand) | View in location tab

Co-located

with COSMIC COSM147733 (G/A) ; HGMD-PUBLIC CM073244

Most severe consequence
Evidence status

Clinical significance

This variation has 10 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

Variation displays