Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.48 (G)
Location

Chromosome 1:20650956 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts, has 2840 individual genotypes and is mentioned in 1 citation.

Variation displays