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rs730880482

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880482(A;G)
Make rs730880482(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position120447845
GeneLAMP2
is asnp
is mentioned by
dbSNPrs730880482
ebirs730880482
HLIrs730880482
Exacrs730880482
Varsomers730880482
Maprs730880482
PheGenIrs730880482
hapmaprs730880482
1000 genomesrs730880482
hgdprs730880482
ensemblrs730880482
gopubmedrs730880482
geneviewrs730880482
scholarrs730880482
googlers730880482
pharmgkbrs730880482
gwascentralrs730880482
openSNPrs730880482
23andMers730880482
23andMe allrs730880482
SNP Nexus

SNPshotrs730880482
SNPdbers730880482
MSV3drs730880482
GWAS Ctlgrs730880482
Max Magnitude0
ClinVar
Risk rs730880482(G;G)
Alt rs730880482(G;G)
Reference rs730880482(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119581700T>C
CLNSRC
CLNACC RCV000157968.1,