Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.06 (C)
Location

Chromosome 12:53720345 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 7 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 21 transcripts and has 3804 individual genotypes.

Variation displays