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 X:119575717 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM051550

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8372, 2010_April_001_225_LAMP2_309060_0011

This variation has 13 HGVS names - click the plus to show

Variation displays