Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 16:50711745 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020655

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: Illumina_ImmunoChip, Illumina_ExomeChip

About this variant

This variant overlaps 22 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays