Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 4:73854481 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.73854481T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 2504 individual genotypes.

Variation displays