Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.18 (C)
Location

Chromosome 1:12263817 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs9430685, rs17880016

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni5

Variation displays