Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 22:36702021 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002810

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4237, NM_002473.4:c.2114G>A

This variation has 3 HGVS names - click the plus to show

Variation displays