Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.13 (A)
Location

Chromosome 9:37429817 (forward strand) | View in location tab

Co-located

with COSMIC COSM4163857 (A/G), COSM4163856 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

Variation displays