Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.32 (G)

Chromosome 16:28487970 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 38 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 42 transcripts and has 2293 individual genotypes.

Variation displays