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rs730880486

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880486(C;C)
Make rs730880486(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position120442640
GeneLAMP2
is asnp
is mentioned by
dbSNPrs730880486
ebirs730880486
HLIrs730880486
Exacrs730880486
Varsomers730880486
Maprs730880486
PheGenIrs730880486
hapmaprs730880486
1000 genomesrs730880486
hgdprs730880486
ensemblrs730880486
gopubmedrs730880486
geneviewrs730880486
scholarrs730880486
googlers730880486
pharmgkbrs730880486
gwascentralrs730880486
openSNPrs730880486
23andMers730880486
23andMe allrs730880486
SNP Nexus

SNPshotrs730880486
SNPdbers730880486
MSV3drs730880486
GWAS Ctlgrs730880486
Max Magnitude0
ClinVar
Risk rs730880486(C;C)
Alt rs730880486(C;C)
Reference rs730880486(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119576495A>G
CLNSRC
CLNACC RCV000157974.1,