Original source

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

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

Chromosome 5:136027886 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

5:g.136027886C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 2532 individual genotypes.

Variation displays