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: 0.20 (A)
Location

Chromosome 22:23285182 (forward strand) | View in location tab

Co-located

with COSMIC COSM3759076 (A/G) ; HGMD-PUBLIC CM057927

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

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