Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.50 (G)
Location

Chromosome 19:10296493 (forward strand) | View in location tab

Co-located

with COSMIC COSM3749448 (G/C)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59589621, rs17852403

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

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays