Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.07 (T)
Location

Chromosome 3:15512242 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

Variation displays