Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.32 (G)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386574212, rs827786

HGVS name

19:g.10289434G>C

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip, Illumina_Human1M-duo, Illumina_ImmunoChip

About this variant

This variant overlaps 13 transcripts, has 2824 individual genotypes and is mentioned in 3 citations.

Variation displays