Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.45 (A)
Location

Chromosome 16:88812323 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs837758, rs57492385

HGVS name

16:g.88812323A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_Human1M-duo

Variation displays