Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: < 0.01 (T)
Location

Chromosome 17:40309098 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.40309098G>T

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 3112 individual genotypes.

Variation displays