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rs727503119

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503119(G;T)
Make rs727503119(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position120446304
GeneLAMP2
is asnp
is mentioned by
dbSNPrs727503119
ebirs727503119
HLIrs727503119
Exacrs727503119
Varsomers727503119
Maprs727503119
PheGenIrs727503119
hapmaprs727503119
1000 genomesrs727503119
hgdprs727503119
ensemblrs727503119
gopubmedrs727503119
geneviewrs727503119
scholarrs727503119
googlers727503119
pharmgkbrs727503119
gwascentralrs727503119
openSNPrs727503119
23andMers727503119
23andMe allrs727503119
SNP Nexus

SNPshotrs727503119
SNPdbers727503119
MSV3drs727503119
GWAS Ctlgrs727503119
Max Magnitude0
ClinVar
Risk rs727503119(A,T;A,T)
Alt rs727503119(A,T;A,T)
Reference rs727503119(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.119580159C>A; NC_000023.10:g.119580159C>T
CLNSRC
CLNACC RCV000150912.1, RCV000157972.1, RCV000157971.1,