Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.33 (G)
Location

Chromosome 5:35871190 (forward strand) | View in location tab

Co-located

with COSMIC COSM149814 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

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

Variation displays