Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.39 (G)
Location

Chromosome 13:27630722 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

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

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 6 transcripts and has 3749 sample genotypes.

Variant displays