Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 12:57057205 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3190098

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

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_Human610_Quad

Variation displays