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rs1057519127

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519127(C;G)
Make rs1057519127(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position68411574
GeneLRP5
is asnp
is mentioned by
dbSNPrs1057519127
dbSNP (classic)rs1057519127
ClinGenrs1057519127
ebirs1057519127
HLIrs1057519127
Exacrs1057519127
Gnomadrs1057519127
Varsomers1057519127
LitVarrs1057519127
Maprs1057519127
PheGenIrs1057519127
Biobankrs1057519127
1000 genomesrs1057519127
hgdprs1057519127
ensemblrs1057519127
geneviewrs1057519127
scholarrs1057519127
googlers1057519127
pharmgkbrs1057519127
gwascentralrs1057519127
openSNPrs1057519127
23andMers1057519127
23andMe allrs1057519127
SNPshotrs1057519127
SNPdbers1057519127
MSV3drs1057519127
GWAS Ctlgrs1057519127
Max Magnitude0
ClinVar
Risk rs1057519127(G;G)
Alt rs1057519127(G;G)
Reference Rs1057519127(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRP5
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.68179042C>G
CLNSRC
CLNACC RCV000415804.1,