Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.15 (T)
Location

Chromosome 16:31315385 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 4 HGVS names - click the plus to show

16:g.31315385C>T
ENST00000567031.1:c.454-9014C>T
ENST00000287497.12:c.1708-5856C>T
ENST00000544665.7:c.1711-5856C>T

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, has 3629 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variant displays