Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R
Location

Chromosome 11:47441675 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM064189

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_286_RAPSN_601592_0007, 10267

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and is associated with 3 phenotypes.

Variant displays