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rs730880490

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880490(A;A)
Make rs730880490(A;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position120469104
GeneLAMP2
is asnp
is mentioned by
dbSNPrs730880490
ebirs730880490
HLIrs730880490
Exacrs730880490
Varsomers730880490
Maprs730880490
PheGenIrs730880490
hapmaprs730880490
1000 genomesrs730880490
hgdprs730880490
ensemblrs730880490
gopubmedrs730880490
geneviewrs730880490
scholarrs730880490
googlers730880490
pharmgkbrs730880490
gwascentralrs730880490
openSNPrs730880490
23andMers730880490
23andMe allrs730880490
SNP Nexus

SNPshotrs730880490
SNPdbers730880490
MSV3drs730880490
GWAS Ctlgrs730880490
Max Magnitude0
ClinVar
Risk rs730880490(A;A)
Alt rs730880490(A;A)
Reference rs730880490(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119602959A>T
CLNSRC
CLNACC RCV000157980.1,