Original source

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

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

Chromosome 14:73186859 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM951073

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

PhenCode ADM_21

This variant has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and is associated with 3 phenotypes.

Variant displays