Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.49 (G)
Location

Chromosome 14:28766331 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

14:g.28766331C>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5

Variation displays