Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.09 (C)
Location

Chromosome 1:247922126 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

1:g.247922126A>C

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 1 transcript and has 2845 sample genotypes.

Variant displays