Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.27 (C)
Location

Chromosome 8:96161256 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_023599

HGVS name

8:g.96161256T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 5 transcripts and has 2506 individual genotypes.

Variation displays