Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060502302

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs1060502302(GAG;TA)
Make rs1060502302(TA;TA)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position120448978
GeneLAMP2
is asnp
is mentioned by
dbSNPrs1060502302
dbSNP (old)rs1060502302
ClinGenrs1060502302
ebirs1060502302
HLIrs1060502302
Exacrs1060502302
Gnomadrs1060502302
Varsomers1060502302
Maprs1060502302
PheGenIrs1060502302
Biobankrs1060502302
1000 genomesrs1060502302
hgdprs1060502302
ensemblrs1060502302
gopubmedrs1060502302
geneviewrs1060502302
scholarrs1060502302
googlers1060502302
pharmgkbrs1060502302
gwascentralrs1060502302
openSNPrs1060502302
23andMers1060502302
23andMe allrs1060502302
SNPshotrs1060502302
SNPdbers1060502302
MSV3drs1060502302
GWAS Ctlgrs1060502302
Max Magnitude0
ClinVar
Risk rs1060502302(TA;TA)
Alt rs1060502302(TA;TA)
Reference Rs1060502302(GAG;GAG)
Significance Pathogenic
Disease Danon disease
Variation info
Gene LAMP2
CLNDBN Danon disease
Reversed 1
HGVS NC_000023.10:g.119582833_119582835delCTCinsTA
CLNSRC
CLNACC RCV000470635.1,