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: 0.34 (G)
Location

Chromosome 19:10289434 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs827786

HGVS name

19:g.10289434G>C

Genotyping chips

This variation has assays on: Illumina_ImmunoChip, Illumina_Cardio-Metabo_Chip, Illumina_1M-duo

Variation displays