Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 13:27667150 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 4 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 7 transcripts and has 3951 individual genotypes.

Variation displays