Original source

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

Alleles
A/G | Ancestral: T | Ambiguity code: R
Location

Chromosome 18:51031780 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

Variation displays