Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 13:51937493 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM023025

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_044486

This variation has 13 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 7 transcripts, has 2504 individual genotypes and is associated with 2 phenotypes.

Variation displays