Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.06 (C)
Location

Chromosome 20:6766417 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.6766417T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 2505 individual genotypes.

Variation displays