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rs730880496

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880496(C;C)
Make rs730880496(C;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position120456770
GeneLAMP2
is asnp
is mentioned by
dbSNPrs730880496
ebirs730880496
HLIrs730880496
Exacrs730880496
Varsomers730880496
Maprs730880496
PheGenIrs730880496
hapmaprs730880496
1000 genomesrs730880496
hgdprs730880496
ensemblrs730880496
gopubmedrs730880496
geneviewrs730880496
scholarrs730880496
googlers730880496
pharmgkbrs730880496
gwascentralrs730880496
openSNPrs730880496
23andMers730880496
23andMe allrs730880496
SNP Nexus

SNPshotrs730880496
SNPdbers730880496
MSV3drs730880496
GWAS Ctlgrs730880496
Max Magnitude0
ClinVar
Risk rs730880496(C;C)
Alt rs730880496(C;C)
Reference rs730880496(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119590625C>G
CLNSRC
CLNACC RCV000157989.2,