Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.49 (A)
Location

Chromosome 11:71435531 (forward strand) | View in location tab

Co-located

with COSMIC COSM329305 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs3184254

This variation has 8 HGVS names - click the plus to show

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

Variation displays