Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 6:98833517 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.98833517G>T

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 1 individual genotype.

Variation displays