Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status


This variation has 12 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 12 transcripts, has 4134 individual genotypes and is mentioned in 41 citations.

Variation displays