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rs1057520861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520861(G;T)
Make rs1057520861(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position169154511
GeneLRP2
is asnp
is mentioned by
dbSNPrs1057520861
dbSNP (old)rs1057520861
ClinGenrs1057520861
ebirs1057520861
HLIrs1057520861
Exacrs1057520861
Gnomadrs1057520861
Varsomers1057520861
LitVarrs1057520861
Maprs1057520861
PheGenIrs1057520861
Biobankrs1057520861
1000 genomesrs1057520861
hgdprs1057520861
ensemblrs1057520861
gopubmedrs1057520861
geneviewrs1057520861
scholarrs1057520861
googlers1057520861
pharmgkbrs1057520861
gwascentralrs1057520861
openSNPrs1057520861
23andMers1057520861
23andMe allrs1057520861
SNPshotrs1057520861
SNPdbers1057520861
MSV3drs1057520861
GWAS Ctlgrs1057520861
Max Magnitude0
ClinVar
Risk rs1057520861(T;T)
Alt rs1057520861(T;T)
Reference Rs1057520861(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRP2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.170011021C>A
CLNSRC
CLNACC RCV000440469.1,