Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.02 (T)

Chromosome 13:48411303 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs17352821

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 3443 sample genotypes and is mentioned in 2 citations.

Variant displays