Original source

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

G/C/T | Ancestral: G | Ambiguity code: B | MAF: 0.37 (C)

Chromosome 14:64227153 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 42 transcripts, has 2865 sample genotypes and is mentioned in 22 citations.

Variant displays