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

Chromosome 11:47448832 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM073304

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10270

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

About this variant

This variant overlaps 13 transcripts and is associated with 2 phenotypes.

Variation displays