Original source

PhenCode is a collaborative project to better understand the relationship between genotype and phenotype in humans (release 04/2014) | View in PhenCode

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

Chromosome 11:47348424 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981322 ; ClinVar rs397516074 (C/T)

Most severe consequence

This variation has 12 HGVS names - click the plus to show

Variation displays