Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: < 0.01 (G)
Location

Chromosome 1:12166212 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.12166212A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 4 transcripts, has 2668 individual genotypes and is mentioned in 2 citations.

Variation displays