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 (G)
Location

Chromosome 6:39357302 (forward strand) | View in location tab

Co-located

with COSMIC COSM150088 (A/G) ; HGMD-PUBLIC CM074911

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 13 chips - click the plus to show

Variation displays