Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 4:74272477 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM984065

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB FDH-1, 193

This variation has 14 HGVS names - click the plus to show

Variation displays