Original source

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

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

Chromosome 11:47463227 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM064189

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_286_RAPSN_601592_0007, 10267

This variation has 8 HGVS names - click the plus to show

Variation displays