Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ambiguity code: Y | MAF: 0.36 (T)
Location

Chromosome 11:18403471 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60322231, rs59107852

This variation has 17 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 25 transcripts and has 2660 individual genotypes.

Variation displays