Original source

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

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

Chromosome 22:29674891 (forward strand) | View in location tab

Co-located

with COSMIC COSM23667 (C/T) ; HGMD-PUBLIC CM941106

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14822, 2009_August_001_069_NF2_607379_0014

This variation has 27 HGVS names - click the plus to show

Variation displays