Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.04 (T)

Chromosome 17:42795422 (forward strand) | View in location tab


with HGMD-PUBLIC CS045336

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs58192643

This variant has 5 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 11 transcripts and has 2775 sample genotypes.

Variant displays