Rs104894857

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894857(C;T)
Make rs104894857(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position120449006
GeneLAMP2
is asnp
is mentioned by
dbSNPrs104894857
Exacrs104894857
PheGenIrs104894857
nextbiors104894857
hapmaprs104894857
1000 genomesrs104894857
hgdprs104894857
ensemblrs104894857
gopubmedrs104894857
geneviewrs104894857
scholarrs104894857
googlers104894857
pharmgkbrs104894857
gwascentralrs104894857
openSNPrs104894857
23andMers104894857
23andMe allrs104894857
SNP Nexus

SNPshotrs104894857
SNPdbers104894857
MSV3drs104894857
OMIM309060
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104894857(T;T)
Alt rs104894857(T;T)
Reference rs104894857(C;C)
Significance Pathogenic
Disease Danon disease
Variation info
Gene LAMP2
CLNDBN Danon disease
Reversed 1
HGVS NC_000023.10:g.119582861G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010662.2,