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rs1064796635

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position120455571
GeneLAMP2
is asnp
is mentioned by
dbSNPrs1064796635
dbSNP (old)rs1064796635
ClinGenrs1064796635
ebirs1064796635
HLIrs1064796635
Exacrs1064796635
Gnomadrs1064796635
Varsomers1064796635
Maprs1064796635
PheGenIrs1064796635
Biobankrs1064796635
1000 genomesrs1064796635
hgdprs1064796635
ensemblrs1064796635
gopubmedrs1064796635
geneviewrs1064796635
scholarrs1064796635
googlers1064796635
pharmgkbrs1064796635
gwascentralrs1064796635
openSNPrs1064796635
23andMers1064796635
23andMe allrs1064796635
SNPshotrs1064796635
SNPdbers1064796635
MSV3drs1064796635
GWAS Ctlgrs1064796635
Max Magnitude0
ClinVar
Risk rs1064796635(T;T)
Alt rs1064796635(T;T)
Reference Rs1064796635(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119589426C>A
CLNSRC
CLNACC RCV000478574.1,