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 22:36292060 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002373, CM010348, CM014588

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

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

About this variant

This variant overlaps 6 transcripts, is associated with 10 phenotypes and is mentioned in 6 citations.

Variation displays