Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (C)
Location

Chromosome 16:23181435 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

16:g.23181435T>C

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 3692 sample genotypes.

Variant displays