Original source

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

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

Chromosome 22:30077466 (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 27 HGVS names - click the plus to show

Variation displays