Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.18 (A)
Location

Chromosome 14:92106583 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 11 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 50 transcripts, has 2505 individual genotypes and is mentioned in 1 citation.

Variation displays