Original source

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

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

Chromosome 12:53074910 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

12:g.53074910T>C

Genotyping chips

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

Variation displays