Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.11 (C)
Location

Chromosome 10:6010681 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

This variant has 2 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 4 transcripts and has 2507 sample genotypes.

Variant displays