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 16:20348858 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM023183

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and is associated with 3 phenotypes.

Variation displays