Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 4:73406760 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM984065

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB FDH-1

This variant has 18 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts, 1 regulatory feature, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays