Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.14 (G)
Location

Chromosome 19:8975282 (forward strand) | View in location tab

Co-located

with COSMIC COSM4132887 (A/G), COSM4132888 (A/G)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

Variation displays