Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.41 (C)
Location

Chromosome 11:2904183 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58682076

HGVS name

11:g.2904183T>C

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni2.5

Variation displays