Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 22:29674882 (forward strand) | View in location tab

Co-located

with COSMIC COSM23876 (G/A) ; HGMD-PUBLIC CM941105

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_068_NF2_607379_0013, 14821

This variation has 54 HGVS names - click the plus to show

Variation displays