Original source

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

Alleles
T/C/G | Ancestral: G | Ambiguity code: B | MAF: 0.13 (C)
Location

Chromosome 16:88875928 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs117055399, rs3167705

This variation has 20 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays