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: 0.25 (G)
Location

Chromosome 10:69382664 (forward strand) | View in location tab

Co-located

with COSMIC COSM4144806 (G/A), COSM4144804 (G/A), COSM4144805 (G/A), COSM4144803 (G/A)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17850368, rs60876495

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

This variation has assays on 10 chips - click the plus to show

Variation displays