Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.35 (G)
Location

Chromosome 16:89770373 (forward strand) | View in location tab

Most severe consequence

 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]

Evidence status

Synonyms

Archive dbSNP rs57637944, rs17226638

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays