Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.32 (T)

Chromosome 11:18026269 (forward strand) | View in location tab


with HGMD-PUBLIC CS034323

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59956346

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 5 transcripts, has 2612 sample genotypes and is mentioned in 57 citations.

Variant displays