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rs876657696

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657696(A;A)
Make rs876657696(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position120455460
GeneLAMP2
is asnp
is mentioned by
dbSNPrs876657696
ebirs876657696
HLIrs876657696
Exacrs876657696
Varsomers876657696
Maprs876657696
PheGenIrs876657696
hapmaprs876657696
1000 genomesrs876657696
hgdprs876657696
ensemblrs876657696
gopubmedrs876657696
geneviewrs876657696
scholarrs876657696
googlers876657696
pharmgkbrs876657696
gwascentralrs876657696
openSNPrs876657696
23andMers876657696
23andMe allrs876657696
SNP Nexus

SNPshotrs876657696
SNPdbers876657696
MSV3drs876657696
GWAS Ctlgrs876657696
Max Magnitude0
ClinVar
Risk rs876657696(A;A)
Alt rs876657696(A;A)
Reference rs876657696(G;G)
Significance Pathogenic
Disease Danon disease
Variation info
Gene LAMP2
CLNDBN Danon disease
Reversed 1
HGVS NC_000023.10:g.119589315C>T
CLNSRC
CLNACC RCV000223450.1,