Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D | MAF: 0.15 (A)
Location

Chromosome 2:85625544 (forward strand) | View in location tab

Co-located

with COSMIC COSM148888 (G/A)

Most severe consequence
Evidence status

Synonyms

This variation has 26 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays