Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 22:29681477 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961040

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14814, 2009_August_001_059_NF2_607379_0006

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

Variation displays