Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.08 (C)
Location

Chromosome 12:42485324 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 5 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1, Affy GeneChip 500K

About this variant

This variant overlaps 10 transcripts and has 3796 sample genotypes.

Variant displays