Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.34 (A)
Location

Chromosome 8:96148852 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 4 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 2508 sample genotypes.

Variant displays