Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.50 (G)
Location

Chromosome 13:51937470 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 7 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, has 2598 sample genotypes, is associated with 2 phenotypes and is mentioned in 3 citations.

Variant displays