Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.02 (C)
Location

Chromosome 12:21788602 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs7297559, rs11547918

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_ExomeChip

Variation displays