Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.26 (C)

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


with HGMD-PUBLIC CR057423

Most severe consequence
Evidence status


Archive dbSNP rs3212034

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

Genotyping chips

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

About this variant

This variant overlaps 22 transcripts, has 1457 individual genotypes and is mentioned in 18 citations.

Variation displays