Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.24 (C)
Location

Chromosome 12:40337381 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17520320, rs17484398

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays