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: 0.49 (A)
Location

Chromosome 17:7078078 (forward strand) | View in location tab

Co-located

with COSMIC COSM4130543 (A/G), COSM4130542 (A/G)

Most severe consequence
Evidence status

This variation has 7 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

Variation displays