Original source

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

Alleles
A/G/T | Ancestral: A | Ambiguity code: D
Location

Chromosome 4:73413589 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM973674, CM995269

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Bergamo, Brest

This variation has 38 HGVS names - click the plus to show

About this variant

This variant overlaps 36 transcripts, is associated with 2 phenotypes and is mentioned in 2 citations.

Variation displays