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rs727504262

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504262(A;A)
Make rs727504262(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position120441895
GeneLAMP2
is asnp
is mentioned by
dbSNPrs727504262
ebirs727504262
HLIrs727504262
Exacrs727504262
Varsomers727504262
Maprs727504262
PheGenIrs727504262
hapmaprs727504262
1000 genomesrs727504262
hgdprs727504262
ensemblrs727504262
gopubmedrs727504262
geneviewrs727504262
scholarrs727504262
googlers727504262
pharmgkbrs727504262
gwascentralrs727504262
openSNPrs727504262
23andMers727504262
23andMe allrs727504262
SNP Nexus

SNPshotrs727504262
SNPdbers727504262
MSV3drs727504262
GWAS Ctlgrs727504262
Max Magnitude0
ClinVar
Risk rs727504262(A;A)
Alt rs727504262(A;A)
Reference rs727504262(G;G)
Significance Probable-Pathogenic
Disease Danon disease
Variation info
Gene LAMP2
CLNDBN Danon disease
Reversed 1
HGVS NC_000023.10:g.119575750C>T
CLNSRC
CLNACC RCV000154245.2,