Original source

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

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

Chromosome 22:29681468 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950859

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14813, 2009_August_001_058_NF2_607379_0005

This variation has 26 HGVS names - click the plus to show

Variation displays