Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 22:29655621 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941100

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_060_NF2_607379_0008, 14816

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

Variation displays