Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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


with dbSNP rs369313054 (T/-)

Most severe consequence
Intron variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 11 HGVS names - 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