Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.36 (G)
Location

Chromosome 11:128780134 (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: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1

About this variant

This variant overlaps 6 transcripts, has 2585 individual genotypes and is mentioned in 1 citation.

Variation displays