Original source

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

A/G/T | Ancestral: A | Ambiguity code: D | MAF: < 0.01 (T)

Chromosome 14:73221080 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs1735103

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 16 transcripts and has 2710 sample genotypes.

Variant displays