Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.02 (A)
Location

Chromosome 8:39919023 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 11 transcripts, has 1347 individual genotypes and is mentioned in 1 citation.

Variation displays