Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.03 (A)
Location

Chromosome 11:47343211 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs16938600, rs12794596

This variation has 7 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_Cardio-Metabo_Chip

Variation displays