Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/T | Ambiguity code: Y
Location

Chromosome 22:36284474 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002374

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4231, NM_002473.4:c.5521G>A

This variation has 5 HGVS names - click the plus to show

Variation displays