Original source

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

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.24 (A)

Chromosome 14:104793397 (forward strand) | View in location tab


with HGMD-PUBLIC CR108282

Most severe consequence
5 prime UTR variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature, has 4134 sample genotypes and is mentioned in 43 citations.

Variant displays