Original source

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

About this variant

This variant overlaps 5 transcripts and is associated with 2 phenotypes.

Variation displays