Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.36 (T)

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


with HGMD-PUBLIC CS034323

Most severe consequence
Evidence status


Archive dbSNP rs59956346

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

Genotyping chips

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

About this variant

This variant overlaps 5 transcripts, has 2566 individual genotypes and is mentioned in 56 citations.

Variation displays