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rs730880485

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880485(C;C)
Make rs730880485(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position120446303
GeneLAMP2
is asnp
is mentioned by
dbSNPrs730880485
ebirs730880485
HLIrs730880485
Exacrs730880485
Varsomers730880485
Maprs730880485
PheGenIrs730880485
hapmaprs730880485
1000 genomesrs730880485
hgdprs730880485
ensemblrs730880485
gopubmedrs730880485
geneviewrs730880485
scholarrs730880485
googlers730880485
pharmgkbrs730880485
gwascentralrs730880485
openSNPrs730880485
23andMers730880485
23andMe allrs730880485
SNP Nexus

SNPshotrs730880485
SNPdbers730880485
MSV3drs730880485
GWAS Ctlgrs730880485
Max Magnitude0
ClinVar
Risk rs730880485(C;C)
Alt rs730880485(C;C)
Reference rs730880485(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119580158A>G
CLNSRC
CLNACC RCV000157973.2,