Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.31 (C)
Location

Chromosome 8:31067041 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 2546 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays