Original source

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

C/A/T | Ancestral: C | Ambiguity code: H | MAF: < 0.01 (T)

Chromosome 4:53377935 (forward strand) | View in location tab


with dbSNP rs758029289 (C/-)

Most severe consequence
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

Variant displays