Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.21 (C)
Location

Chromosome 14:30877806 (forward strand) | View in location tab

Co-located

with dbSNP rs369313054 (T/-)

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 11 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 12 transcripts, has 2506 sample genotypes and is associated with 1 phenotype.

Variant displays