Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.25 (C)
Location

Chromosome 3:58415590 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57965226, rs2234820

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni5, Illumina_ImmunoChip

Variation displays