Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.22 (C)
Location

Chromosome 9:712060 (forward strand) | View in location tab

Co-located

with COSMIC COSM1132465 (G/C), COSM1132467 (G/C)

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

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

Variation displays