Original source

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

Alleles
T/C/G|Ancestral: T|Ambiguity code: B
Location

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

Co-located variant

HGMD-PUBLIC CM984065

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB FDH-1

HGVS names

This variant has 38 HGVS names - Show

About this variant

This variant overlaps 30 transcripts, 1 regulatory feature, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays