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rs1057517940

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517940(C;T)
Make rs1057517940(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position120441748
GeneLAMP2
is asnp
is mentioned by
dbSNPrs1057517940
dbSNP (old)rs1057517940
ClinGenrs1057517940
ebirs1057517940
HLIrs1057517940
Exacrs1057517940
Gnomadrs1057517940
Varsomers1057517940
LitVarrs1057517940
Maprs1057517940
PheGenIrs1057517940
Biobankrs1057517940
1000 genomesrs1057517940
hgdprs1057517940
ensemblrs1057517940
gopubmedrs1057517940
geneviewrs1057517940
scholarrs1057517940
googlers1057517940
pharmgkbrs1057517940
gwascentralrs1057517940
openSNPrs1057517940
23andMers1057517940
23andMe allrs1057517940
SNPshotrs1057517940
SNPdbers1057517940
MSV3drs1057517940
GWAS Ctlgrs1057517940
Max Magnitude0
ClinVar
Risk rs1057517940(T;T)
Alt rs1057517940(T;T)
Reference Rs1057517940(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119575603G>A
CLNSRC
CLNACC RCV000414477.1,