Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 22:29681443 (forward strand) | View in location tab

Co-located

with COSMIC COSM1142979 (G/C) ; HGMD-PUBLIC CM941107

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_070_NF2_607379_0015, 14823

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

About this variant

This variant overlaps 13 transcripts and is associated with 2 phenotypes.

Variation displays