Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.16 (G)
Location

Chromosome 1:219914120 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs74139242

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 2506 individual genotypes.

Variation displays