This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ancestral: A | Ambiguity code: N
Location

Chromosome 16:20348652 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM034987, CM023184

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 27 HGVS names - click the plus to show

About this variant

This variant overlaps 37 transcripts and is associated with 5 phenotypes.

Variation displays