Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 22:36295069 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002372

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_002473.4:c.3493C>T, 4232

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

Variation displays