This variation has been flagged

Variation has more than 3 different alleles

Original source

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

C/A/G/T | Ancestral: C | Ambiguity code: N | MAF: < 0.01 (G)

Chromosome 11:5225678 (forward strand) | View in location tab


with HGMD-PUBLIC CM860012, CM900124, CM930381 ; PhenCode HbVar.951 (C/A), HbVar.510 (C/T), HbVar.509 (C/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 8 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 16 transcripts, has 2504 individual genotypes, is associated with 12 phenotypes and is mentioned in 24 citations.

Variation displays