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 1:16986546 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 9 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature and has 3 sample genotypes.

Variant displays