Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.17 (G)
Location

Chromosome 1:153258885 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.153258885C>G

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 3693 individual genotypes.

Variation displays