Original source

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

A/G | Ambiguity code: R | MAF: 0.46 (G)

Chromosome 16:28483029 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 36 HGVS names - click the plus to show

About this variant

This variant overlaps 38 transcripts and has 1098 individual genotypes.

Variation displays