Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.49 (G)

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


with COSMIC COSM3749448 (G/C)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs59589621, rs17852403

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

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 4 transcripts and has 2507 sample genotypes.

Variant displays