Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.41 (A)
Location

Chromosome 19:844077 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs643029

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5

Variation displays