This variant 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

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

Chromosome 16:3243403 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM055415, CM981245

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 7 synonyms - click the plus to show

This variant has 63 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 48 transcripts, has 2504 sample genotypes, is associated with 5 phenotypes and is mentioned in 1 citation.

Variant displays