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rs397516740

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516740(A;A)
Make rs397516740(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position120455461
GeneLAMP2
is asnp
is mentioned by
dbSNPrs397516740
ebirs397516740
HLIrs397516740
Exacrs397516740
Varsomers397516740
Maprs397516740
PheGenIrs397516740
hapmaprs397516740
1000 genomesrs397516740
hgdprs397516740
ensemblrs397516740
gopubmedrs397516740
geneviewrs397516740
scholarrs397516740
googlers397516740
pharmgkbrs397516740
gwascentralrs397516740
openSNPrs397516740
23andMers397516740
23andMe allrs397516740
SNP Nexus

SNPshotrs397516740
SNPdbers397516740
MSV3drs397516740
GWAS Ctlgrs397516740
Max Magnitude0
ClinVar
Risk rs397516740(A;A)
Alt rs397516740(A;A)
Reference rs397516740(G;G)
Significance Pathogenic
Disease Danon disease not provided
Variation info
Gene LAMP2
CLNDBN Danon disease not provided
Reversed 1
HGVS NC_000023.10:g.119589316C>T
CLNSRC ClinVar
CLNACC RCV000037412.3, RCV000157963.1,