Rs104894859

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894859(C;C)
Make rs104894859(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position120441862
GeneLAMP2
is asnp
is mentioned by
dbSNPrs104894859
Exacrs104894859
PheGenIrs104894859
nextbiors104894859
hapmaprs104894859
1000 genomesrs104894859
hgdprs104894859
ensemblrs104894859
gopubmedrs104894859
geneviewrs104894859
scholarrs104894859
googlers104894859
pharmgkbrs104894859
gwascentralrs104894859
openSNPrs104894859
23andMers104894859
23andMe allrs104894859
SNP Nexus

SNPshotrs104894859
SNPdbers104894859
MSV3drs104894859
OMIM309060
Desc
Variant0011
Relatedalso
ClinVar
Risk rs104894859(C;C)
Alt rs104894859(C;C)
Reference rs104894859(T;T)
Significance Pathogenic
Disease Danon disease
Variation info
Gene LAMP2
CLNDBN Danon disease
Reversed 1
HGVS NC_000023.10:g.119575717A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010664.3,