Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.29 (C)

Chromosome 14:103712930 (forward strand) | View in location tab


with HGMD-PUBLIC CR057423

Most severe consequence
Splice region variant
Evidence status


Archive dbSNP rs3212034

This variant has 14 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 22 transcripts, has 2857 sample genotypes and is mentioned in 20 citations.

Variant displays