Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.29 (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

Variation displays