This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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 CM014588, CM010348, CM002373

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

Variation displays