Original source

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

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

Chromosome 22:30067894 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930517

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14809, 2009_August_001_057_NF2_607379_0001

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

Variation displays