Original source

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

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

Chromosome 11:47448924 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020757

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10262, 2010_April_001_284_RAPSN_601592_0002

This variation has 9 HGVS names - click the plus to show

Variation displays