Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: < 0.01 (A)

Chromosome 4:73412007 (forward strand) | View in location tab


with HGMD-PUBLIC CM970078, CM920015

Most severe consequence
Evidence status

Clinical significance


LSDB FDH-3, 178, FDH-2

This variation has 36 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

About this variant

This variant overlaps 34 transcripts, has 1092 individual genotypes, is associated with 4 phenotypes and is mentioned in 4 citations.

Variation displays