Original source

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

Alleles
C/A/G|Ancestral: C|Ambiguity code: V
Location

Chromosome 4:73413602 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB OrebroSW

HGVS names

This variant has 38 HGVS names - Show

About this variant

This variant overlaps 36 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays