Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variant

HGMD-PUBLIC CM941100

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 14816, 2009_August_001_060_NF2_607379_0008

HGVS names

This variant has 26 HGVS names - Show

About this variant

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

Variant displays